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rs10735781

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) >1.11x risk
(C;G) 1.11x risk
(G;G) common
ReferenceGRCh38 38.1/141
Chromosome1
Position92655550
GeneEVI5
is asnp
is mentioned by
dbSNPrs10735781
ebirs10735781
HLIrs10735781
Exacrs10735781
Varsomers10735781
Maprs10735781
PheGenIrs10735781
hapmaprs10735781
1000 genomesrs10735781
hgdprs10735781
ensemblrs10735781
gopubmedrs10735781
geneviewrs10735781
scholarrs10735781
googlers10735781
pharmgkbrs10735781
gwascentralrs10735781
openSNPrs10735781
23andMers10735781
23andMe allrs10735781
SNP Nexus

SNPshotrs10735781
SNPdbers10735781
MSV3drs10735781
GWAS Ctlgrs10735781
GMAF0.3535
Max Magnitude
? (C;C) (C;G) (G;G) 28
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]



[PMID 19865102OA-icon.png] Multiple sclerosis susceptibility alleles in African Americans

[PMID 20546594OA-icon.png] An application of Random Forests to a genome-wide association dataset: methodological considerations & new findings.


GET Evidence
rs10735781
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.570312
summary