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rs3745672

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs3745672(C;C)
Make rs3745672(C;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position12035555
GeneCNTFR, ZNF433
is asnp
is mentioned by
dbSNPrs3745672
ebirs3745672
HLIrs3745672
Exacrs3745672
Varsomers3745672
Maprs3745672
PheGenIrs3745672
hapmaprs3745672
1000 genomesrs3745672
hgdprs3745672
ensemblrs3745672
gopubmedrs3745672
geneviewrs3745672
scholarrs3745672
googlers3745672
pharmgkbrs3745672
gwascentralrs3745672
openSNPrs3745672
23andMers3745672
23andMe allrs3745672
SNP Nexus

SNPshotrs3745672
SNPdbers3745672
MSV3drs3745672
GWAS Ctlgrs3745672
GMAF0.06152
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20598377]
Trait Multiple sclerosis
Title Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis
Risk Allele
P-val 0.000001
Odds Ratio 7.39 [3.32-16.47]