rs8093763
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs8093763(A;A) |
Make rs8093763(A;G) |
Make rs8093763(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 18 |
Position | 59836146 |
is a | snp |
is | mentioned by |
dbSNP | rs8093763 |
dbSNP (classic) | rs8093763 |
ClinGen | rs8093763 |
ebi | rs8093763 |
HLI | rs8093763 |
Exac | rs8093763 |
Gnomad | rs8093763 |
Varsome | rs8093763 |
LitVar | rs8093763 |
Map | rs8093763 |
PheGenI | rs8093763 |
Biobank | rs8093763 |
1000 genomes | rs8093763 |
hgdp | rs8093763 |
ensembl | rs8093763 |
geneview | rs8093763 |
scholar | rs8093763 |
rs8093763 | |
pharmgkb | rs8093763 |
gwascentral | rs8093763 |
openSNP | rs8093763 |
23andMe | rs8093763 |
SNPshot | rs8093763 |
SNPdbe | rs8093763 |
MSV3d | rs8093763 |
GWAS Ctlg | rs8093763 |
GMAF | 0.2759 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 21106707] A genetic variant near the PMAIP1/Noxa gene is associated with increased bleomycin sensitivity