rs1327301
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1327301(C;C) |
Make rs1327301(C;T) |
Make rs1327301(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 51467205 |
is a | snp |
is | mentioned by |
dbSNP | rs1327301 |
dbSNP (classic) | rs1327301 |
ClinGen | rs1327301 |
ebi | rs1327301 |
HLI | rs1327301 |
Exac | rs1327301 |
Gnomad | rs1327301 |
Varsome | rs1327301 |
LitVar | rs1327301 |
Map | rs1327301 |
PheGenI | rs1327301 |
Biobank | rs1327301 |
1000 genomes | rs1327301 |
hgdp | rs1327301 |
ensembl | rs1327301 |
geneview | rs1327301 |
scholar | rs1327301 |
rs1327301 | |
pharmgkb | rs1327301 |
gwascentral | rs1327301 |
openSNP | rs1327301 |
23andMe | rs1327301 |
SNPshot | rs1327301 |
SNPdbe | rs1327301 |
MSV3d | rs1327301 |
GWAS Ctlg | rs1327301 |
GMAF | 0.2098 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 19767753] |
Trait | Prostate cancer |
Title | Identification of seven new prostate cancer susceptibility loci through a genome-wide association study |
Risk Allele | T |
P-val | 2E-10 |
Odds Ratio | NR NR |
[PMID 19549809] Fine-mapping and family-based association analyses of prostate cancer risk variants at Xp11.