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rs4368253

From SNPedia

Orientationplus
Stabilizedplus
Make rs4368253(C;C)
Make rs4368253(C;T)
Make rs4368253(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position59955055
is asnp
is mentioned by
dbSNPrs4368253
ebirs4368253
HLIrs4368253
Exacrs4368253
Varsomers4368253
Maprs4368253
PheGenIrs4368253
hapmaprs4368253
1000 genomesrs4368253
hgdprs4368253
ensemblrs4368253
gopubmedrs4368253
geneviewrs4368253
scholarrs4368253
googlers4368253
pharmgkbrs4368253
gwascentralrs4368253
openSNPrs4368253
23andMers4368253
23andMe allrs4368253
SNP Nexus

SNPshotrs4368253
SNPdbers4368253
MSV3drs4368253
GWAS Ctlgrs4368253
GMAF0.3264
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23770605OA-icon.png]
Trait Chronic lymphocytic leukemia
Title Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia.
Risk Allele C
P-val 3E-8
Odds Ratio 1.19 [1.12-1.27]