Standard
Digit length ratio
FLI1 · rs10790969
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
C/C
Published research associates this genotype with typical/baseline likelihood of Digit length ratio — no copies of the reported risk allele.
C/T
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Digit length ratio.
T/T
Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Digit length ratio compared to the general population.
Source
Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero
Warrington NM,
Shevroja E,
Hemani G,
Hysi PG,
Jiang Y,
Auton A,
Boer CG,
Mangino M,
Wang CA,
Kemp JP,
McMahon G,
Medina-Gomez C
and 18 more — show all
Hickey M,
Trajanoska K,
Wolke D,
Ikram MA,
Montgomery GW,
Felix JF,
Wright MJ,
Mackey DA,
Jaddoe VW,
Martin NG,
Tung JY,
Davey Smith G,
Pennell CE,
Spector TD,
van Meurs J,
Rivadeneira F,
Medland SE,
Evans DM
Human molecular genetics · 2018 · PMID 29659830 · open access
Questions about rs10790969
What is rs10790969?
rs10790969 is a single position in the genome, in or near the FLI1 gene. Published research associates it with digit length ratio. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs10790969 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 rs10790969 come from?
GWAS Catalog, Hum Mol Genet 2018, PMID:29659830. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
← See all variants