rs934635
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs934635(A;A) |
Make rs934635(A;G) |
Make rs934635(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 51186580 |
is a | snp |
is | mentioned by |
dbSNP | rs934635 |
dbSNP (classic) | rs934635 |
ClinGen | rs934635 |
ebi | rs934635 |
HLI | rs934635 |
Exac | rs934635 |
Gnomad | rs934635 |
Varsome | rs934635 |
LitVar | rs934635 |
Map | rs934635 |
PheGenI | rs934635 |
Biobank | rs934635 |
1000 genomes | rs934635 |
hgdp | rs934635 |
ensembl | rs934635 |
geneview | rs934635 |
scholar | rs934635 |
rs934635 | |
pharmgkb | rs934635 |
gwascentral | rs934635 |
openSNP | rs934635 |
23andMe | rs934635 |
SNPshot | rs934635 |
SNPdbe | rs934635 |
MSV3d | rs934635 |
GWAS Ctlg | rs934635 |
GMAF | 0.1175 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 24590773] Germline variants in the CYP19A1 gene are related to specific adverse events in aromatase inhibitor users: a substudy of Dutch patients in the TEAM trial