rs2055109
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2055109(A;A) |
Make rs2055109(A;G) |
Make rs2055109(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 87418182 |
is a | snp |
is | mentioned by |
dbSNP | rs2055109 |
dbSNP (classic) | rs2055109 |
ClinGen | rs2055109 |
ebi | rs2055109 |
HLI | rs2055109 |
Exac | rs2055109 |
Gnomad | rs2055109 |
Varsome | rs2055109 |
LitVar | rs2055109 |
Map | rs2055109 |
PheGenI | rs2055109 |
Biobank | rs2055109 |
1000 genomes | rs2055109 |
hgdp | rs2055109 |
ensembl | rs2055109 |
geneview | rs2055109 |
scholar | rs2055109 |
rs2055109 | |
pharmgkb | rs2055109 |
gwascentral | rs2055109 |
openSNP | rs2055109 |
23andMe | rs2055109 |
SNPshot | rs2055109 |
SNPdbe | rs2055109 |
MSV3d | rs2055109 |
GWAS Ctlg | rs2055109 |
GMAF | 0.1515 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 22366784] Common variants at 11q12, 10q26 and 3p11.2 are associated with prostate cancer susceptibility in Japanese