rs6969502
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6969502(A;A) |
Make rs6969502(A;G) |
Make rs6969502(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 22712807 |
is a | snp |
is | mentioned by |
dbSNP | rs6969502 |
dbSNP (classic) | rs6969502 |
ClinGen | rs6969502 |
ebi | rs6969502 |
HLI | rs6969502 |
Exac | rs6969502 |
Gnomad | rs6969502 |
Varsome | rs6969502 |
LitVar | rs6969502 |
Map | rs6969502 |
PheGenI | rs6969502 |
Biobank | rs6969502 |
1000 genomes | rs6969502 |
hgdp | rs6969502 |
ensembl | rs6969502 |
geneview | rs6969502 |
scholar | rs6969502 |
rs6969502 | |
pharmgkb | rs6969502 |
gwascentral | rs6969502 |
openSNP | rs6969502 |
23andMe | rs6969502 |
SNPshot | rs6969502 |
SNPdbe | rs6969502 |
MSV3d | rs6969502 |
GWAS Ctlg | rs6969502 |
GMAF | 0.4366 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
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[PMID 19965896] PTGS2 and IL6 Genetic Variation and Risk of Breast and Prostate Cancer: results from the Breast and Prostate Cancer Cohort Consortium (BPC3)