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Heel bone mineral density

FAM129B · rs72767980

Where this position leads

Condition: Heel Bone Mineral Density

rs72767980 Condition: Heel Bone Mineral Density Heel Bone Mineral Density Condition rs72767980 rs72767980 FAM129B

What each result means

C/C Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Heel bone mineral density compared to the general population.
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Heel bone mineral density.
T/T Published research associates this genotype with typical/baseline likelihood of Heel bone mineral density — no copies of the reported risk allele.
Source
Identification of 153 new loci associated with heel bone mineral density and functional involvement of GPC6 in osteoporosis
Kemp JP, Morris JA, Medina-Gomez C, Forgetta V, Warrington NM, Youlten SE, Zheng J, Gregson CL, Grundberg E, Trajanoska K, Logan JG, Pollard AS
and 26 more — show all
Sparkes PC, Ghirardello EJ, Allen R, Leitch VD, Butterfield NC, Komla-Ebri D, Adoum AT, Curry KF, White JK, Kussy F, Greenlaw KM, Xu C, Harvey NC, Cooper C, Adams DJ, Greenwood CMT, Maurano MT, Kaptoge S, Rivadeneira F, Tobias JH, Croucher PI, Ackert-Bicknell CL, Bassett JHD, Williams GR, Richards JB, Evans DM
Nature genetics · 2017 · PMID 28869591 · open access

Questions about rs72767980

What is rs72767980?

rs72767980 is a single position in the genome, in or near the FAM129B gene. Published research associates it with heel bone mineral density. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs72767980 linked to?

On MyGeneLog this position is linked to Heel Bone Mineral Density. The research behind each link, and its sources, are set out on that condition page.

Does having rs72767980 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 rs72767980 come from?

GWAS Catalog, Nat Genet 2017, PMID:28869591. 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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