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rs7169431

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs7169431(A;A)
Make rs7169431(A;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position56048698
is asnp
is mentioned by
dbSNPrs7169431
ebirs7169431
HLIrs7169431
Exacrs7169431
Varsomers7169431
Maprs7169431
PheGenIrs7169431
hapmaprs7169431
1000 genomesrs7169431
hgdprs7169431
ensemblrs7169431
gopubmedrs7169431
geneviewrs7169431
scholarrs7169431
googlers7169431
pharmgkbrs7169431
gwascentralrs7169431
openSNPrs7169431
23andMers7169431
23andMe allrs7169431
SNP Nexus

SNPshotrs7169431
SNPdbers7169431
MSV3drs7169431
GWAS Ctlgrs7169431
GMAF0.1221
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20062064]
Trait Chronic lymphocytic leukemia
Title Common variants at 2q37.3, 8q24.21, 15q21.3 abd 16q24.1 influence chronic lymphocytic leukemia risk
Risk Allele A
P-val 5E-7
Odds Ratio 1.36 [1.21-1.53]


[PMID 20855867] Inherited genetic susceptibility to monoclonal B-cell lymphocytosis