rs6949149
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs6949149(G;T) |
Make rs6949149(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 22709538 |
is a | snp |
is | mentioned by |
dbSNP | rs6949149 |
dbSNP (classic) | rs6949149 |
ClinGen | rs6949149 |
ebi | rs6949149 |
HLI | rs6949149 |
Exac | rs6949149 |
Gnomad | rs6949149 |
Varsome | rs6949149 |
LitVar | rs6949149 |
Map | rs6949149 |
PheGenI | rs6949149 |
Biobank | rs6949149 |
1000 genomes | rs6949149 |
hgdp | rs6949149 |
ensembl | rs6949149 |
geneview | rs6949149 |
scholar | rs6949149 |
rs6949149 | |
pharmgkb | rs6949149 |
gwascentral | rs6949149 |
openSNP | rs6949149 |
23andMe | rs6949149 |
SNPshot | rs6949149 |
SNPdbe | rs6949149 |
MSV3d | rs6949149 |
GWAS Ctlg | rs6949149 |
GMAF | 0.2631 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
[PMID 19965896] PTGS2 and IL6 Genetic Variation and Risk of Breast and Prostate Cancer: results from the Breast and Prostate Cancer Cohort Consortium (BPC3)