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rs11164838

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) >1.11x risk
(C;T) 1.11x risk
(T;T) 0 common
ReferenceGRCh38 38.1/141
Chromosome1
Position92929821
GeneFAM69A
is asnp
is mentioned by
dbSNPrs11164838
ebirs11164838
HLIrs11164838
Exacrs11164838
Varsomers11164838
Maprs11164838
PheGenIrs11164838
hapmaprs11164838
1000 genomesrs11164838
hgdprs11164838
ensemblrs11164838
gopubmedrs11164838
geneviewrs11164838
scholarrs11164838
googlers11164838
pharmgkbrs11164838
gwascentralrs11164838
openSNPrs11164838
23andMers11164838
23andMe allrs11164838
SNP Nexus

SNPshotrs11164838
SNPdbers11164838
MSV3drs11164838
GWAS Ctlgrs11164838
GMAF0.4408
Max Magnitude0
? (C;C) (C;T) (T;T) 28
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]



GET Evidence
rs11164838
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.34375
summary