rs12014709
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12014709(G;G) |
Make rs12014709(G;T) |
Make rs12014709(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 67718624 |
Gene | AR |
is a | snp |
is | mentioned by |
dbSNP | rs12014709 |
dbSNP (classic) | rs12014709 |
ClinGen | rs12014709 |
ebi | rs12014709 |
HLI | rs12014709 |
Exac | rs12014709 |
Gnomad | rs12014709 |
Varsome | rs12014709 |
LitVar | rs12014709 |
Map | rs12014709 |
PheGenI | rs12014709 |
Biobank | rs12014709 |
1000 genomes | rs12014709 |
hgdp | rs12014709 |
ensembl | rs12014709 |
geneview | rs12014709 |
scholar | rs12014709 |
rs12014709 | |
pharmgkb | rs12014709 |
gwascentral | rs12014709 |
openSNP | rs12014709 |
23andMe | rs12014709 |
SNPshot | rs12014709 |
SNPdbe | rs12014709 |
MSV3d | rs12014709 |
GWAS Ctlg | rs12014709 |
GMAF | 0.1475 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
[PMID 20880698] Polymorphic variation in the androgen receptor gene: Association with risk of testicular germ cell cancer and metastatic disease