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rs7745098

From SNPedia

Orientationplus
Stabilizedplus
Make rs7745098(C;C)
Make rs7745098(C;T)
Make rs7745098(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position135093866
is asnp
is mentioned by
dbSNPrs7745098
ebirs7745098
HLIrs7745098
Exacrs7745098
Varsomers7745098
Maprs7745098
PheGenIrs7745098
hapmaprs7745098
1000 genomesrs7745098
hgdprs7745098
ensemblrs7745098
gopubmedrs7745098
geneviewrs7745098
scholarrs7745098
googlers7745098
pharmgkbrs7745098
gwascentralrs7745098
openSNPrs7745098
23andMers7745098
23andMe allrs7745098
SNP Nexus

SNPshotrs7745098
SNPdbers7745098
MSV3drs7745098
GWAS Ctlgrs7745098
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 24149102]
Trait Hodgkin's lymphoma
Title Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphoma.
Risk Allele G
P-val 3E-9
Odds Ratio 1.21 [1.14-1.29]