Rs10735781

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is asnp
is mentioned by
dbSNPrs10735781
hapmaprs10735781
hgdprs10735781
ensemblrs10735781
gopubmedrs10735781
scholarrs10735781
googlers10735781
pharmgkbrs10735781
hgvbaseg2prs10735781
medrefsnprs10735781
23andMers10735781
SNP Nexus

GeneEVI5
Chromosome1
Orientationplus
Position92893694
GenotypeEffect
rs10735781(C;C)>1.11x risk
rs10735781(C;G)1.11x risk
rs10735781(G;G)common


Genotypes Magnitude Summary
Rs10735781(C;C) >1.11x risk
Rs10735781(C;G) 1.11x risk
Rs10735781(G;G) common
rs10735781 has been reported in a large study to be associated with multiple sclerosis.

The risk allele (oriented to the dbSNP entry) is (G); the odds ratio associated with this allele is 1.11 (CI 1.05-1.18). [PMID 17660530]

? (C;C) (C;G) (G;G)
PharmGKBPA162356169
Name
AnnotationIn a replicated GWAS of U.K. and U.S. case/parent trios, this variant was shown to be associated with multiple sclerosis risk.
GeneEVI5
Featue
EvidencePubMed ID:17660530
Drugs
DiseasesMultiple Sclerosis
Curation LevelCurated