Standard
Pulse pressure
AMH · rs10407022
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 each result means
G/G
Published research associates this genotype with typical/baseline likelihood of Pulse pressure — no copies of the reported risk allele.
G/T
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Pulse pressure.
T/T
Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Pulse pressure compared to the general population.
Source
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
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Tragante V
and 198 more — show all
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Tuomi T,
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Palotie A,
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Salomaa V,
Alam DS,
Shafi Majumder AA,
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McCarthy MI,
Poulter N,
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Amouyel P,
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Kuulasmaa K,
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Nature genetics · 2016 · PMID 27618447 · open access
Questions about rs10407022
What is rs10407022?
rs10407022 is a single position in the genome, in or near the AMH gene. Published research associates it with pulse pressure. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs10407022 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 rs10407022 come from?
GWAS Catalog, Nat Genet 2016, PMID:27618447. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
← See all variants