Cryptic phenotype that captures autosomal dominant polycystic kidney disease severity
WNT2B · rs12037987
0 145225Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot5Amazon2Apple2China (ByteDance, Huawei, Baidu…)0Others5Total14Counted 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 the study found
Who was studied 308,095 European ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.015 higher (95% confidence interval 0.011-0.019); p = 6 × 10−11.
Where it sits Chromosome 1, band 1p13.2 — in an intron of WNT2B.
What each result means
C/CTwo copies of the version the research linked to Cryptic phenotype that captures autosomal dominant polycystic kidney disease severity. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/TOne copy of the version the research linked to Cryptic phenotype that captures autosomal dominant polycystic kidney disease severity. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Cryptic phenotype that captures autosomal dominant polycystic kidney disease severity. This is the starting point the study compared everyone against.
Nature communications · 2022 · PMID 35760791 · open access
Questions about rs12037987
What is rs12037987?
rs12037987 is a single position in the genome, in or near the WNT2B gene. Published research associates it with cryptic phenotype that captures autosomal dominant polycystic kidney disease severity. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs12037987 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 rs12037987 come from?
GWAS Catalog, Nature communications 2022, PMID:35760791. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 145225Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot5Amazon2Apple2China (ByteDance, Huawei, Baidu…)0Others5Total14Counted 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.