Difference between revisions of "Rs10411210"

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(Created page with "<table border="1" cellpadding="1" cellspacing="1" style="width:1000px"> <tbody> <tr><th>항목</th><th>한글</th><th>영문</th></tr> <tr><td style="text-align: center;">ID</...")
 
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<table border="1" cellpadding="1" cellspacing="1" style="width:1000px">
 
<table border="1" cellpadding="1" cellspacing="1" style="width:1000px">
<tbody>
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<tbody>
<tr><th>항목</th><th>한글</th><th>영문</th></tr>
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<tr>
<tr><td style="text-align: center;">ID</td> <td colspan=2 style="text-align: center;">rs10411210</td></tr>
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<th>항목</th>
<tr><td style="text-align: center;">염색체</td> <td colspan=2 style="text-align: center;">chr19</td></tr>
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<th>한글</th>
<tr><td style="text-align: center;">염색체상 위치</td> <td colspan=2 style="text-align: center;">33532300</td> </tr>
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<th>영문</th>
<tr><td style="text-align: center;">표준게놈 유전형</td> <td colspan=2 style="text-align: center;">C</td> </tr>
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</tr>
<tr><td style="text-align: center;">위험 유전형</td> <td colspan=2 style="text-align: center;">C</td> </tr>
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<tr>
<tr><td style="text-align: center;">변이 종류</td> <td></td> <td>intron_variant</td> </tr>
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<td style="text-align:center">ID</td>
<tr><td style="text-align: center;">유전자</td> <td>[[RHPN2]]</td> <td>[[RHPN2]]</td> </tr>
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<td colspan="2" style="text-align:center">rs10411210</td>
<tr><td style="text-align: center;">인족별 분포</td> <td></td> <td></td> </tr>
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</tr>
<tr><td style="text-align: center;">관련 표현형</td> <td>[[결장(직장)암]]</td> <td>[[Colorectal cancer]]</td> </tr>
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<tr>
<tr><td style="text-align: center;">설명</td> <td></td> <td></td> </tr>
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<td style="text-align:center">염색체</td>
<tr><td style="text-align: center;">관련 논문</td> <td></td> <td></td> </tr>
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<td colspan="2" style="text-align:center">chr19</td>
<tr><td style="text-align: center;">비고</td> <td>표준게놈은 hg19 기준입니다.</td> <td></td> </tr>
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</tr>
</tbody>
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<tr>
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<td style="text-align:center">염색체상 위치</td>
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<td colspan="2" style="text-align:center">33532300</td>
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</tr>
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<tr>
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<td style="text-align:center">표준게놈 유전형</td>
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<td colspan="2" style="text-align:center">C</td>
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</tr>
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<tr>
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<td style="text-align:center">위험 유전형</td>
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<td colspan="2" style="text-align:center">C</td>
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</tr>
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<tr>
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<td style="text-align:center">변이 종류</td>
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<td>&nbsp;</td>
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<td>intron_variant</td>
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</tr>
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<tr>
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<td style="text-align:center">유전자</td>
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<td>[[RHPN2]]</td>
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<td>[[RHPN2]]</td>
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</tr>
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<tr>
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<td style="text-align:center">인족별 분포</td>
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<td><img alt="" src="/ckfinder/userfiles/images/rs10411210.PNG" style="height:324px; width:405px" /></td>
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<td>&nbsp;</td>
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</tr>
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<tr>
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<td style="text-align:center">관련 표현형</td>
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<td>[[결장(직장)암]]</td>
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<td>[[Colorectal cancer]]</td>
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</tr>
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<tr>
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<td style="text-align:center">설명</td>
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<td>&nbsp;</td>
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<td>&nbsp;</td>
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</tr>
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<tr>
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<td style="text-align:center">관련 논문</td>
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<td>&nbsp;</td>
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<td>[<a href="https://www.ncbi.nlm.nih.gov/pubmed/21119214?dopt=Abstract" rel="nofollow">PMID 21119214</a><a href="https://www.snpedia.com/index.php/File:OA-icon.png"><img alt="OA-icon.png" src="https://media.snpedia.com/images/5/5b/OA-icon.png" style="height:15px; width:15px" /></a>] Colorectal Cancer Susceptibility Loci in a Population-Based Study: Associations with Morphological Parameters
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<p><br />
 +
[<a href="https://www.ncbi.nlm.nih.gov/pubmed/22363440?dopt=Abstract" rel="nofollow">PMID 22363440</a><a href="https://www.snpedia.com/index.php/File:OA-icon.png"><img alt="OA-icon.png" src="https://media.snpedia.com/images/5/5b/OA-icon.png" style="height:15px; width:15px" /></a>] cis-Expression QTL Analysis of Established Colorectal Cancer Risk Variants in Colon Tumors and Adjacent Normal Tissue</p>
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<p><br />
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[<a href="https://www.ncbi.nlm.nih.gov/pubmed/22367214?dopt=Abstract" rel="nofollow">PMID 22367214</a><a href="https://www.snpedia.com/index.php/File:OA-icon.png"><img alt="OA-icon.png" src="https://media.snpedia.com/images/5/5b/OA-icon.png" style="height:15px; width:15px" /></a>] Characterization of gene-environment interactions for colorectal cancer susceptibility loci</p>
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<p>[<a href="https://www.ncbi.nlm.nih.gov/pubmed/19639606?dopt=Abstract" rel="nofollow">PMID 19639606</a><a href="https://www.snpedia.com/index.php/File:OA-icon.png"><img alt="OA-icon.png" src="https://media.snpedia.com/images/5/5b/OA-icon.png" style="height:15px; width:15px" /></a>] Correcting &quot;winner&#39;s curse&quot; in odds ratios from genomewide association findings for major complex human diseases.</p>
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<p>[<a href="https://www.ncbi.nlm.nih.gov/pubmed/20501757?dopt=Abstract" rel="nofollow">PMID 20501757</a><a href="https://www.snpedia.com/index.php/File:OA-icon.png"><img alt="OA-icon.png" src="https://media.snpedia.com/images/5/5b/OA-icon.png" style="height:15px; width:15px" /></a>] Low-penetrance susceptibility variants in familial colorectal cancer.</p>
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<p>[<a href="https://www.ncbi.nlm.nih.gov/pubmed/21071539?dopt=Abstract" rel="nofollow">PMID 21071539</a><a href="https://www.snpedia.com/index.php/File:OA-icon.png"><img alt="OA-icon.png" src="https://media.snpedia.com/images/5/5b/OA-icon.png" style="height:15px; width:15px" /></a>] Generalizability and epidemiologic characterization of eleven colorectal cancer GWAS hits in multiple populations.</p>
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<p>[<a href="https://www.ncbi.nlm.nih.gov/pubmed/21314996?dopt=Abstract" rel="nofollow">PMID 21314996</a><a href="https://www.snpedia.com/index.php/File:OA-icon.png"><img alt="OA-icon.png" src="https://media.snpedia.com/images/5/5b/OA-icon.png" style="height:15px; width:15px" /></a>] Systematic search for enhancer elements and somatic allelic imbalance at seven low-penetrance colorectal cancer predisposition loci.</p>
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<p>[<a href="https://www.ncbi.nlm.nih.gov/pubmed/22045029?dopt=Abstract" rel="nofollow">PMID 22045029</a>] Relationship between 16 susceptibility loci and colorectal cancer phenotype in 3146 patients.</p>
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<p>[<a href="https://www.ncbi.nlm.nih.gov/pubmed/22235025?dopt=Abstract" rel="nofollow">PMID 22235025</a>] Susceptibility genetic variants associated with early-onset colorectal cancer.</p>
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<p><br />
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[<a href="https://www.ncbi.nlm.nih.gov/pubmed/23359760?dopt=Abstract" rel="nofollow">PMID 23359760</a><a href="https://www.snpedia.com/index.php/File:OA-icon.png"><img alt="OA-icon.png" src="https://media.snpedia.com/images/5/5b/OA-icon.png" style="height:15px; width:15px" /></a>] Single-nucleotide polymorphism associations for colorectal cancer in southern chinese population</p>
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<p><br />
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[<a href="https://www.ncbi.nlm.nih.gov/pubmed/22848671?dopt=Abstract" rel="nofollow">PMID 22848671</a><a href="https://www.snpedia.com/index.php/File:OA-icon.png"><img alt="OA-icon.png" src="https://media.snpedia.com/images/5/5b/OA-icon.png" style="height:15px; width:15px" /></a>] Association of eleven common, low-penetrance colorectal cancer susceptibility genetic variants at six risk loci with clinical outcome.</p>
 +
 
 +
<p><br />
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[<a href="https://www.ncbi.nlm.nih.gov/pubmed/22999960?dopt=Abstract" rel="nofollow">PMID 22999960</a><a href="https://www.snpedia.com/index.php/File:OA-icon.png"><img alt="OA-icon.png" src="https://media.snpedia.com/images/5/5b/OA-icon.png" style="height:15px; width:15px" /></a>] Much of the genetic risk of colorectal cancer is likely to be mediated through susceptibility to adenomas.</p>
 +
 
 +
<p><br />
 +
[<a href="https://www.ncbi.nlm.nih.gov/pubmed/23434150?dopt=Abstract" rel="nofollow">PMID 23434150</a><a href="https://www.snpedia.com/index.php/File:OA-icon.png"><img alt="OA-icon.png" src="https://media.snpedia.com/images/5/5b/OA-icon.png" style="height:15px; width:15px" /></a>] Are the common genetic variants associated with colorectal cancer risk for DNA mismatch repair gene mutation carriers?</p>
 +
 
 +
<p><br />
 +
[<a href="https://www.ncbi.nlm.nih.gov/pubmed/24854447?dopt=Abstract" rel="nofollow">PMID 24854447</a>] Association analysis of colorectal cancer susceptibility variants with gastric cancer in a Chinese Han population</p>
 +
 
 +
<p><br />
 +
[<a href="https://www.ncbi.nlm.nih.gov/pubmed/25021488?dopt=Abstract" rel="nofollow">PMID 25021488</a>] PWE-010 The Association Of Tgfb Signalling Pathway Gene Polymorphisms With Colorectal Cancer Risk: A Meta-analysis</p>
 +
</td>
 +
</tr>
 +
<tr>
 +
<td style="text-align:center">비고</td>
 +
<td>표준게놈은 hg19 기준입니다.</td>
 +
<td>&nbsp;</td>
 +
</tr>
 +
</tbody>
 
</table>
 
</table>

Revision as of 23:00, 15 January 2018

항목 한글 영문
ID rs10411210
염색체 chr19
염색체상 위치 33532300
표준게놈 유전형 C
위험 유전형 C
변이 종류   intron_variant
유전자 RHPN2 RHPN2
인족별 분포  
관련 표현형 결장(직장)암 Colorectal cancer
설명    
관련 논문   [PMID 21119214OA-icon.png] Colorectal Cancer Susceptibility Loci in a Population-Based Study: Associations with Morphological Parameters


[PMID 22363440OA-icon.png] cis-Expression QTL Analysis of Established Colorectal Cancer Risk Variants in Colon Tumors and Adjacent Normal Tissue


[PMID 22367214OA-icon.png] Characterization of gene-environment interactions for colorectal cancer susceptibility loci

[PMID 19639606OA-icon.png] Correcting "winner's curse" in odds ratios from genomewide association findings for major complex human diseases.

[PMID 20501757OA-icon.png] Low-penetrance susceptibility variants in familial colorectal cancer.

[PMID 21071539OA-icon.png] Generalizability and epidemiologic characterization of eleven colorectal cancer GWAS hits in multiple populations.

[PMID 21314996OA-icon.png] Systematic search for enhancer elements and somatic allelic imbalance at seven low-penetrance colorectal cancer predisposition loci.

[PMID 22045029] Relationship between 16 susceptibility loci and colorectal cancer phenotype in 3146 patients.

[PMID 22235025] Susceptibility genetic variants associated with early-onset colorectal cancer.


[PMID 23359760OA-icon.png] Single-nucleotide polymorphism associations for colorectal cancer in southern chinese population


[PMID 22848671OA-icon.png] Association of eleven common, low-penetrance colorectal cancer susceptibility genetic variants at six risk loci with clinical outcome.


[PMID 22999960OA-icon.png] Much of the genetic risk of colorectal cancer is likely to be mediated through susceptibility to adenomas.


[PMID 23434150OA-icon.png] Are the common genetic variants associated with colorectal cancer risk for DNA mismatch repair gene mutation carriers?


[PMID 24854447] Association analysis of colorectal cancer susceptibility variants with gastric cancer in a Chinese Han population


[PMID 25021488] PWE-010 The Association Of Tgfb Signalling Pathway Gene Polymorphisms With Colorectal Cancer Risk: A Meta-analysis

비고 표준게놈은 hg19 기준입니다.