Rs4763655

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is asnp
is mentioned by
dbSNPrs4763655
hapmaprs4763655
hgdprs4763655
ensemblrs4763655
gopubmedrs4763655
scholarrs4763655
googlers4763655
pharmgkbrs4763655
hgvbaseg2prs4763655
medrefsnprs4763655
23andMers4763655
SNP Nexus

GeneKLRB1
Chromosome12
Orientationplus
Position9646844
GenotypeEffect
rs4763655(A;A)>1.10x risk
rs4763655(A;G)1.10x risk
rs4763655(G;G)common


Genotypes Magnitude Summary
Rs4763655(A;A) >1.10x risk
Rs4763655(A;G) 1.10x risk
Rs4763655(G;G) 00 common
rs4763655 has been reported in a large study to be associated with multiple sclerosis.

The risk allele (oriented to the dbSNP entry) is (A); the odds ratio associated with this allele is 1.10 (CI 1.04-1.17). [PMID 17660530]

? (A;A) (A;G) (G;G)
PharmGKBPA162356171
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.
GeneKLRB1
Featue
EvidencePubMed ID:17660530
Drugs
DiseasesMultiple Sclerosis
Curation LevelCurated