Rs11164838

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is asnp
is mentioned by
dbSNPrs11164838
hapmaprs11164838
hgdprs11164838
ensemblrs11164838
gopubmedrs11164838
scholarrs11164838
googlers11164838
pharmgkbrs11164838
hgvbaseg2prs11164838
medrefsnprs11164838
23andMers11164838
SNP Nexus

GeneFAM69A
Chromosome1
Orientationplus
Position93167965
GenotypeEffect
rs11164838(C;C)>1.11x risk
rs11164838(C;T)1.11x risk
rs11164838(T;T)common


Genotypes Magnitude Summary
Rs11164838(C;C) >1.11x risk
Rs11164838(C;T) 1.11x risk
Rs11164838(T;T) 00 common
rs11164838 has been reported in a large study to be associated with multiple sclerosis.

The risk allele (oriented to the dbSNP entry) is (C); the odds ratio associated with this allele is 1.12 (CI 1.05-1.18). [PMID 17660530]

? (C;C) (C;T) (T;T)
PharmGKBPA162356167
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.
GeneFAM69A
Featue
EvidencePubMed ID:17660530
Drugs
DiseasesMultiple Sclerosis
Curation LevelCurated