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rs3780792

From SNPedia

Orientationplus
Stabilizedplus
Make rs3780792(A;A)
Make rs3780792(A;G)
Make rs3780792(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position133970221
GeneVAV2
is asnp
is mentioned by
dbSNPrs3780792
ebirs3780792
HLIrs3780792
Exacrs3780792
Varsomers3780792
Maprs3780792
PheGenIrs3780792
hapmaprs3780792
1000 genomesrs3780792
hgdprs3780792
ensemblrs3780792
gopubmedrs3780792
geneviewrs3780792
scholarrs3780792
googlers3780792
pharmgkbrs3780792
gwascentralrs3780792
openSNPrs3780792
23andMers3780792
23andMe allrs3780792
SNP Nexus

SNPshotrs3780792
SNPdbers3780792
MSV3drs3780792
GWAS Ctlgrs3780792
GMAF0.23
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20598377]
Trait Multiple sclerosis
Title Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis
Risk Allele G
P-val 0.000001
Odds Ratio 1.60 [1.32-1.92]