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rs4979427

From SNPedia

Orientationplus
Make rs4979427(C;C)
Make rs4979427(C;T)
Make rs4979427(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position114561146
GeneLOC105376229
is asnp
is mentioned by
dbSNPrs4979427
ebirs4979427
HLIrs4979427
Exacrs4979427
Varsomers4979427
Maprs4979427
PheGenIrs4979427
hapmaprs4979427
1000 genomesrs4979427
hgdprs4979427
ensemblrs4979427
gopubmedrs4979427
geneviewrs4979427
scholarrs4979427
googlers4979427
pharmgkbrs4979427
gwascentralrs4979427
openSNPrs4979427
23andMers4979427
23andMe allrs4979427
SNP Nexus

SNPshotrs4979427
SNPdbers4979427
MSV3drs4979427
GWAS Ctlgrs4979427
Max Magnitude
? (C;C) (C;T) (T;T) 28

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