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rs4662834

From SNPedia

Orientationplus
Stabilizedplus
Make rs4662834(A;A)
Make rs4662834(A;G)
Make rs4662834(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position128721268
is asnp
is mentioned by
dbSNPrs4662834
ebirs4662834
HLIrs4662834
Exacrs4662834
Varsomers4662834
Maprs4662834
PheGenIrs4662834
hapmaprs4662834
1000 genomesrs4662834
hgdprs4662834
ensemblrs4662834
gopubmedrs4662834
geneviewrs4662834
scholarrs4662834
googlers4662834
pharmgkbrs4662834
gwascentralrs4662834
openSNPrs4662834
23andMers4662834
23andMe allrs4662834
SNP Nexus

SNPshotrs4662834
SNPdbers4662834
MSV3drs4662834
GWAS Ctlgrs4662834
GMAF0.3985
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21106707OA-icon.png]
Trait
Title A genetic variant near the PMAIP1/Noxa gene is associated with increased bleomycin sensitivity
Risk Allele A
P-val 0.000005
Odds Ratio 0.0800 [0.04-0.11] fewer chromatid breaks