Membrane-associated progesterone receptor component 2 protein levels (SomaScan ID:21696-80)
PC · rs2077432
0 422Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple0China (ByteDance, Huawei, Baidu…)0Others2Total4Counted 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 191 Shetland Isles origin ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.891 lower (95% confidence interval 0.59-1.2); p = 2 × 10−17.
Where it sits Chromosome 11, band 11q13.2 — in an intron of PC.
What each result means
C/CNo copy of the version the research linked to Membrane-associated progesterone receptor component 2 protein levels (SomaScan ID:21696-80). This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Membrane-associated progesterone receptor component 2 protein levels (SomaScan ID:21696-80). That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Membrane-associated progesterone receptor component 2 protein levels (SomaScan ID:21696-80). That is the strongest link of the three results. A link in a study is not a diagnosis.
Communications biology · 2025 · PMID 40883583 · open access
Questions about rs2077432
What is rs2077432?
rs2077432 is a single position in the genome, in or near the PC gene. Published research associates it with membrane-associated progesterone receptor component 2 protein levels (somascan id:21696-80). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs2077432 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 rs2077432 come from?
GWAS Catalog, Communications biology 2025, PMID:40883583. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 422Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple0China (ByteDance, Huawei, Baidu…)0Others2Total4Counted 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.
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