0 453226223124Reads by AI crawlersClaude3ChatGPT2Google · Gemini0Perplexity2Meta AI6Microsoft · Copilot2Amazon2Apple3China (ByteDance, Huawei, Baidu…)1ByteDance (Doubao)1Others24Total45Counted by the name each crawler declares; requests found to be impersonating one are left out. Google · Gemini includes Googlebot, the search crawler whose index Google also uses for its AI features. Other search engines and bots are under Others.
Who was studied 22,775 East Asian ancestry cases, 47,731 East Asian ancestry controls.
The effect
Each copy of the T allele carried 1.10 times the odds of Colorectal cancer (95% confidence interval 1.07-1.13); p = 2 × 10−12.
How common The T allele had a frequency of about 62% in the people studied.
Where it sits Chromosome 3, band 3q22.2 — in the 5′ untranslated region of SLCO2A1.
What ClinVar records
ClassificationBenign; criteria provided, multiple submitters, no conflicts (2 of 4 stars, 2 submitters), last evaluated 2018-11-12.
ClinVar record 1287290NC_000003.12:g.134029945T>C
What this is ClinVar's aggregate record for this position (as of its 2026-10-19 release), not a result about you. A classification describes the variant against the condition named, as laboratories submitted it. Whether a person carries this variant, and what that would mean for them, is a question for a clinical test and a genetic counsellor.
What each result means
C/CNo copy of the version the research linked to Colorectal cancer. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Colorectal cancer. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Colorectal cancer. That is the strongest link of the three results. A link in a study is not a diagnosis.
rs113569514 is a single position in the genome, in or near the SLCO2A1 gene. Published research associates it with colorectal cancer. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs113569514 linked to?
On MyGeneLog this position is linked to Colorectal Cancer. The research behind each link, and its sources, are set out on that condition page.
Does having rs113569514 mean I will get this?
No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.
Where does the information about rs113569514 come from?
GWAS Catalog, Gastroenterology 2018, PMID:30529582. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 453226223124Reads by AI crawlersClaude3ChatGPT2Google · Gemini0Perplexity2Meta AI6Microsoft · Copilot2Amazon2Apple3China (ByteDance, Huawei, Baidu…)1ByteDance (Doubao)1Others24Total45Counted by the name each crawler declares; requests found to be impersonating one are left out. Google · Gemini includes Googlebot, the search crawler whose index Google also uses for its AI features. Other search engines and bots are under Others.
Quoting this page
Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.
Colorectal cancer (rs113569514). MyGeneLog™. https://www.mygenelog.com/variants/rs113569514