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rs1036935

From SNPedia

Orientationminus
Stabilizedplus
Make rs1036935(C;C)
Make rs1036935(C;T)
Make rs1036935(T;T)
ReferenceGRCh38 38.1/142
Chromosome18
Position47843534
is asnp
is mentioned by
dbSNPrs1036935
ebirs1036935
HLIrs1036935
Exacrs1036935
Varsomers1036935
Maprs1036935
PheGenIrs1036935
hapmaprs1036935
1000 genomesrs1036935
hgdprs1036935
ensemblrs1036935
gopubmedrs1036935
geneviewrs1036935
scholarrs1036935
googlers1036935
pharmgkbrs1036935
gwascentralrs1036935
openSNPrs1036935
23andMers1036935
23andMe allrs1036935
SNP Nexus

SNPshotrs1036935
SNPdbers1036935
MSV3drs1036935
GWAS Ctlgrs1036935
GMAF0.1896
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 0.000002
Odds Ratio 1.22 [1.12-1.32]


[PMID 21554262] Common genetic variation at 15q25.2 impacts on chronic lymphocytic leukaemia risk.

Leukemia