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rs2503875

From SNPedia

Orientationplus
Stabilizedplus
Make rs2503875(A;A)
Make rs2503875(A;G)
Make rs2503875(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position43318601
is asnp
is mentioned by
dbSNPrs2503875
ebirs2503875
HLIrs2503875
Exacrs2503875
Varsomers2503875
Maprs2503875
PheGenIrs2503875
hapmaprs2503875
1000 genomesrs2503875
hgdprs2503875
ensemblrs2503875
gopubmedrs2503875
geneviewrs2503875
scholarrs2503875
googlers2503875
pharmgkbrs2503875
gwascentralrs2503875
openSNPrs2503875
23andMers2503875
23andMe allrs2503875
SNP Nexus

SNPshotrs2503875
SNPdbers2503875
MSV3drs2503875
GWAS Ctlgrs2503875
GMAF0.286
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 A
P-val 2E-7
Odds Ratio 1.66 [1.37-2.00]


[PMID 20532249OA-icon.png] Haplotype analysis reveals a possible founder effect of RET mutation R114H for Hirschsprung's disease in the Chinese population.