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rs7851259

From SNPedia

Orientationplus
Make rs7851259(A;A)
Make rs7851259(A;G)
Make rs7851259(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position114563056
GeneLOC105376229
is asnp
is mentioned by
dbSNPrs7851259
ebirs7851259
HLIrs7851259
Exacrs7851259
Varsomers7851259
Maprs7851259
PheGenIrs7851259
hapmaprs7851259
1000 genomesrs7851259
hgdprs7851259
ensemblrs7851259
gopubmedrs7851259
geneviewrs7851259
scholarrs7851259
googlers7851259
pharmgkbrs7851259
gwascentralrs7851259
openSNPrs7851259
23andMers7851259
23andMe allrs7851259
SNP Nexus

SNPshotrs7851259
SNPdbers7851259
MSV3drs7851259
GWAS Ctlgrs7851259
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 26312577] Bivariate Genome-Wide Association Study Implicates ATP6V1G1 as a Novel Pleiotropic Locus Underlying Osteoporosis and Age at Menarche