1 251222216Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity1Meta AI2Microsoft · Copilot0Amazon2Apple2China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others16Total25Counted 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 556 European ancestry cases, 2,338 European ancestry controls.
The effect
Each copy of the G allele carried 3.83 times the odds of Idiopathic membranous nephropathy; p = 5 × 10−71.
How common The G allele had a frequency of about 11% in the people studied.
Where it sits Chromosome 6, band 6p21.32 — a missense change in TSBP1.
What each result means
G/GTwo copies of the version the research linked to Idiopathic membranous nephropathy. That is the strongest link of the three results. A link in a study is not a diagnosis.
G/TOne copy of the version the research linked to Idiopathic membranous nephropathy. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Idiopathic membranous nephropathy. This is the starting point the study compared everyone against.
The New England journal of medicine · 2011 · PMID 21323541
Questions about rs7775397
What is rs7775397?
rs7775397 is a single position in the genome, in or near the c6orf10 gene. Published research associates it with idiopathic membranous nephropathy. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs7775397 linked to?
On MyGeneLog this position is linked to Idiopathic Membranous Nephropathy. The research behind each link, and its sources, are set out on that condition page.
Does having rs7775397 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 rs7775397 come from?
GWAS Catalog, The New England journal of medicine 2011, PMID:21323541. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
1 251222216Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity1Meta AI2Microsoft · Copilot0Amazon2Apple2China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others16Total25Counted 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.