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rs10982287

From SNPedia

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ReferenceGRCh38.p2 38.2/144
Chromosome9
Position114551935
is asnp
is mentioned by
dbSNPrs10982287
ebirs10982287
HLIrs10982287
Exacrs10982287
Varsomers10982287
Maprs10982287
PheGenIrs10982287
hapmaprs10982287
1000 genomesrs10982287
hgdprs10982287
ensemblrs10982287
gopubmedrs10982287
geneviewrs10982287
scholarrs10982287
googlers10982287
pharmgkbrs10982287
gwascentralrs10982287
openSNPrs10982287
23andMers10982287
23andMe allrs10982287
SNP Nexus

SNPshotrs10982287
SNPdbers10982287
MSV3drs10982287
GWAS Ctlgrs10982287
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