rs767199
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs767199(A;A) |
Make rs767199(A;G) |
Make rs767199(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 51248190 |
Gene | CYP19A1 |
is a | snp |
is | mentioned by |
dbSNP | rs767199 |
dbSNP (classic) | rs767199 |
ClinGen | rs767199 |
ebi | rs767199 |
HLI | rs767199 |
Exac | rs767199 |
Gnomad | rs767199 |
Varsome | rs767199 |
LitVar | rs767199 |
Map | rs767199 |
PheGenI | rs767199 |
Biobank | rs767199 |
1000 genomes | rs767199 |
hgdp | rs767199 |
ensembl | rs767199 |
geneview | rs767199 |
scholar | rs767199 |
rs767199 | |
pharmgkb | rs767199 |
gwascentral | rs767199 |
openSNP | rs767199 |
23andMe | rs767199 |
SNPshot | rs767199 |
SNPdbe | rs767199 |
MSV3d | rs767199 |
GWAS Ctlg | rs767199 |
GMAF | 0.3517 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 19064562] Genetic variation in CYP19A1 and risk of breast cancer and fibrocystic breast conditions among women in Shanghai, China.