0 11Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon0Apple0China (ByteDance, Huawei, Baidu…)0Others1Total1Counted 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 5,662 Pakistani ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.0406 lower (95% confidence interval 0.028-0.053); p = 3 × 10−10.
Where it sits Chromosome 14, band 14q23.2 — in a non-coding transcript of EIF2S2P1.
What each result means
C/CNo copy of the version the research linked to Sphingomyelin(32:1)_[M+H]1+ levels. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Sphingomyelin(32:1)_[M+H]1+ levels. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Sphingomyelin(32:1)_[M+H]1+ levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
rs73267621 is a single position in the genome, in or near the EIF2S2P1 gene. Published research associates it with sphingomyelin(32:1)_[m+h]1+ levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs73267621 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 rs73267621 come from?
GWAS Catalog, BMC medicine 2021, PMID:34503513. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 11Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon0Apple0China (ByteDance, Huawei, Baidu…)0Others1Total1Counted 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.