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rs8093763

From SNPedia

Orientationplus
Stabilizedplus
Make rs8093763(A;A)
Make rs8093763(A;G)
Make rs8093763(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position59836146
is asnp
is mentioned by
dbSNPrs8093763
ebirs8093763
HLIrs8093763
Exacrs8093763
Varsomers8093763
Maprs8093763
PheGenIrs8093763
hapmaprs8093763
1000 genomesrs8093763
hgdprs8093763
ensemblrs8093763
gopubmedrs8093763
geneviewrs8093763
scholarrs8093763
googlers8093763
pharmgkbrs8093763
gwascentralrs8093763
openSNPrs8093763
23andMers8093763
23andMe allrs8093763
SNP Nexus

SNPshotrs8093763
SNPdbers8093763
MSV3drs8093763
GWAS Ctlgrs8093763
GMAF0.2759
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 21106707OA-icon.png] A genetic variant near the PMAIP1/Noxa gene is associated with increased bleomycin sensitivity