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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 0.057 higher (95% confidence interval 0.039-0.075); p = 3 × 10−10.
Where it sits Chromosome 3, band 3q23 — between genes, 1.8 kb from HLMR1.
What each result means
C/CNo copy of the version the research linked to Phosphatidate(44:6)_[M+OAc]1-/Phosphatidylglycerol(43:6)_[M-H]1- levels. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Phosphatidate(44:6)_[M+OAc]1-/Phosphatidylglycerol(43:6)_[M-H]1- levels. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Phosphatidate(44:6)_[M+OAc]1-/Phosphatidylglycerol(43:6)_[M-H]1- levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
rs7650847 is a single position in the genome, in or near the near HLMR1 gene. Published research associates it with phosphatidate(44:6)_[m+oac]1-/phosphatidylglycerol(43:6)_[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 rs7650847 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 rs7650847 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.
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