rs7851259
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7851259(A;A) |
Make rs7851259(A;G) |
Make rs7851259(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 9 |
Position | 114563056 |
Gene | LOC105376229 |
is a | snp |
is | mentioned by |
dbSNP | rs7851259 |
dbSNP (classic) | rs7851259 |
ClinGen | rs7851259 |
ebi | rs7851259 |
HLI | rs7851259 |
Exac | rs7851259 |
Gnomad | rs7851259 |
Varsome | rs7851259 |
LitVar | rs7851259 |
Map | rs7851259 |
PheGenI | rs7851259 |
Biobank | rs7851259 |
1000 genomes | rs7851259 |
hgdp | rs7851259 |
ensembl | rs7851259 |
geneview | rs7851259 |
scholar | rs7851259 |
rs7851259 | |
pharmgkb | rs7851259 |
gwascentral | rs7851259 |
openSNP | rs7851259 |
23andMe | rs7851259 |
SNPshot | rs7851259 |
SNPdbe | rs7851259 |
MSV3d | rs7851259 |
GWAS Ctlg | rs7851259 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
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[PMID 26312577] Bivariate Genome-Wide Association Study Implicates ATP6V1G1 as a Novel Pleiotropic Locus Underlying Osteoporosis and Age at Menarche