Standard
Coffee consumption
HECTD4 · rs144504271
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
A/A
Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Coffee consumption compared to the general population.
A/G
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Coffee consumption.
G/G
Published research associates this genotype with typical/baseline likelihood of Coffee consumption — no copies of the reported risk allele.
Source
A genome-wide association study in the Japanese population identifies the 12q24 locus for habitual coffee consumption: The J-MICC Study
Nakagawa-Senda H,
Hachiya T,
Shimizu A,
Hosono S,
Oze I,
Watanabe M,
Matsuo K,
Ito H,
Hara M,
Nishida Y,
Endoh K,
Kuriki K
and 24 more — show all
Katsuura-Kamano S,
Arisawa K,
Nindita Y,
Ibusuki R,
Suzuki S,
Hosono A,
Mikami H,
Nakamura Y,
Takashima N,
Nakamura Y,
Kuriyama N,
Ozaki E,
Furusyo N,
Ikezaki H,
Nakatochi M,
Sasakabe T,
Kawai S,
Okada R,
Hishida A,
Naito M,
Wakai K,
Momozawa Y,
Kubo M,
Tanaka H
Scientific reports · 2018 · PMID 29367735 · open access
Questions about rs144504271
What is rs144504271?
rs144504271 is a single position in the genome, in or near the HECTD4 gene. Published research associates it with coffee consumption. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs144504271 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 rs144504271 come from?
GWAS Catalog, Sci Rep 2018, PMID:29367735. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
← See all variants