rs5945372
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs5945372(A;A) |
Make rs5945372(A;C) |
Make rs5945372(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 153400456 |
Gene | LOC105373379 |
is a | snp |
is | mentioned by |
dbSNP | rs5945372 |
dbSNP (classic) | rs5945372 |
ClinGen | rs5945372 |
ebi | rs5945372 |
HLI | rs5945372 |
Exac | rs5945372 |
Gnomad | rs5945372 |
Varsome | rs5945372 |
LitVar | rs5945372 |
Map | rs5945372 |
PheGenI | rs5945372 |
Biobank | rs5945372 |
1000 genomes | rs5945372 |
hgdp | rs5945372 |
ensembl | rs5945372 |
geneview | rs5945372 |
scholar | rs5945372 |
rs5945372 | |
pharmgkb | rs5945372 |
gwascentral | rs5945372 |
openSNP | rs5945372 |
23andMe | rs5945372 |
SNPshot | rs5945372 |
SNPdbe | rs5945372 |
MSV3d | rs5945372 |
GWAS Ctlg | rs5945372 |
GMAF | 0.3676 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 19549809] Fine-Mapping and Family-Based Association Analyses of Prostate Cancer Risk Variants at Xp11