rs2219968
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2219968(A;A) |
Make rs2219968(A;G) |
Make rs2219968(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 78044423 |
is a | snp |
is | mentioned by |
dbSNP | rs2219968 |
dbSNP (classic) | rs2219968 |
ClinGen | rs2219968 |
ebi | rs2219968 |
HLI | rs2219968 |
Exac | rs2219968 |
Gnomad | rs2219968 |
Varsome | rs2219968 |
LitVar | rs2219968 |
Map | rs2219968 |
PheGenI | rs2219968 |
Biobank | rs2219968 |
1000 genomes | rs2219968 |
hgdp | rs2219968 |
ensembl | rs2219968 |
geneview | rs2219968 |
scholar | rs2219968 |
rs2219968 | |
pharmgkb | rs2219968 |
gwascentral | rs2219968 |
openSNP | rs2219968 |
23andMe | rs2219968 |
SNPshot | rs2219968 |
SNPdbe | rs2219968 |
MSV3d | rs2219968 |
GWAS Ctlg | rs2219968 |
GMAF | 0.3554 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22219177] |
Trait | |
Title | A genome-wide search for loci interacting with known prostate cancer risk-associated genetic variants. |
Risk Allele | |
P-val | 6E-7 |
Odds Ratio | 1.3000 None |