rs4979427
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4979427(C;C) |
Make rs4979427(C;T) |
Make rs4979427(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 9 |
Position | 114561146 |
Gene | LOC105376229 |
is a | snp |
is | mentioned by |
dbSNP | rs4979427 |
dbSNP (classic) | rs4979427 |
ClinGen | rs4979427 |
ebi | rs4979427 |
HLI | rs4979427 |
Exac | rs4979427 |
Gnomad | rs4979427 |
Varsome | rs4979427 |
LitVar | rs4979427 |
Map | rs4979427 |
PheGenI | rs4979427 |
Biobank | rs4979427 |
1000 genomes | rs4979427 |
hgdp | rs4979427 |
ensembl | rs4979427 |
geneview | rs4979427 |
scholar | rs4979427 |
rs4979427 | |
pharmgkb | rs4979427 |
gwascentral | rs4979427 |
openSNP | rs4979427 |
23andMe | rs4979427 |
SNPshot | rs4979427 |
SNPdbe | rs4979427 |
MSV3d | rs4979427 |
GWAS Ctlg | rs4979427 |
Max Magnitude | 0 |
? | (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