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rs305061

From SNPedia

Orientationplus
Stabilizedplus
Make rs305061(C;C)
Make rs305061(C;T)
Make rs305061(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position85942053
is asnp
is mentioned by
dbSNPrs305061
ebirs305061
HLIrs305061
Exacrs305061
Varsomers305061
Maprs305061
PheGenIrs305061
hapmaprs305061
1000 genomesrs305061
hgdprs305061
ensemblrs305061
gopubmedrs305061
geneviewrs305061
scholarrs305061
googlers305061
pharmgkbrs305061
gwascentralrs305061
openSNPrs305061
23andMers305061
23andMe allrs305061
SNP Nexus

SNPshotrs305061
SNPdbers305061
MSV3drs305061
GWAS Ctlgrs305061
GMAF0.2346
Max Magnitude
? (C;C) (C;T) (T;T) 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 T
P-val 4E-7
Odds Ratio 1.22 [1.12-1.32]


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

GWAS snp
PMID [PMID 22700719OA-icon.png]
Trait
Title Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia.
Risk Allele
P-val 9E-8
Odds Ratio 1.3300 None