0 26221172236Reads by AI crawlersClaude2ChatGPT2Google · Gemini1Perplexity1Meta AI7Microsoft · Copilot2Amazon2Apple3China (ByteDance, Huawei, Baidu…)0Others6Total26Counted 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.
Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What ClinVar records
ClassificationBenign; criteria provided, multiple submitters, no conflicts (2 of 4 stars, 2 submitters), last evaluated 2021-05-13.
ClinVar record 1272274NM_001127392.3(MYRF):c.2572+42A>G
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
A/ANo copy of the version the research linked to Plasma omega-3 polyunsaturated fatty acid levels (alphalinolenic acid). This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Plasma omega-3 polyunsaturated fatty acid levels (alphalinolenic acid). That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Plasma omega-3 polyunsaturated fatty acid levels (alphalinolenic acid). That is the strongest link of the three results. A link in a study is not a diagnosis.
rs509360 is a single position in the genome, in or near the MYRF gene. Published research associates it with plasma omega-3 polyunsaturated fatty acid levels (alphalinolenic acid). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs509360 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 rs509360 come from?
GWAS Catalog, Genes Nutr 2015, PMID:26584805. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 26221172236Reads by AI crawlersClaude2ChatGPT2Google · Gemini1Perplexity1Meta AI7Microsoft · Copilot2Amazon2Apple3China (ByteDance, Huawei, Baidu…)0Others6Total26Counted 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.