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rs708547

From SNPedia

Orientationminus
Stabilizedminus
Make rs708547(A;A)
Make rs708547(A;G)
Make rs708547(G;G)
ReferenceGRCh38 38.1/142
Chromosome4
Position56955143
is asnp
is mentioned by
dbSNPrs708547
dbSNP (classic)rs708547
ClinGenrs708547
ebirs708547
HLIrs708547
Exacrs708547
Gnomadrs708547
Varsomers708547
LitVarrs708547
Maprs708547
PheGenIrs708547
Biobankrs708547
1000 genomesrs708547
hgdprs708547
ensemblrs708547
geneviewrs708547
scholarrs708547
googlers708547
pharmgkbrs708547
gwascentralrs708547
openSNPrs708547
23andMers708547
SNPshotrs708547
SNPdbers708547
MSV3drs708547
GWAS Ctlgrs708547
GMAF0.1492
Max Magnitude0
? (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 9E-7
Odds Ratio 0.1800 [0.11-0.24] fewer chromatid breaks