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rs6680578

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) >1.11x risk
(A;T) 1.11x risk
(T;T) common
ReferenceGRCh38 38.1/141
Chromosome1
Position92711321
GeneEVI5
is asnp
is mentioned by
dbSNPrs6680578
ebirs6680578
HLIrs6680578
Exacrs6680578
Varsomers6680578
Maprs6680578
PheGenIrs6680578
hapmaprs6680578
1000 genomesrs6680578
hgdprs6680578
ensemblrs6680578
gopubmedrs6680578
geneviewrs6680578
scholarrs6680578
googlers6680578
pharmgkbrs6680578
gwascentralrs6680578
openSNPrs6680578
23andMers6680578
23andMe allrs6680578
SNP Nexus

SNPshotrs6680578
SNPdbers6680578
MSV3drs6680578
GWAS Ctlgrs6680578
GMAF0.3558
Max Magnitude
? (A;A) (A;T) (T;T) 28
rs6680578 has been reported in a large study to be associated with multiple sclerosis.

The risk allele (oriented to the dbSNP entry) is (T); the odds ratio associated with this allele is 1.11 (CI 1.04-1.17). [PMID 17660530]



[PMID 20087403OA-icon.png] Tag-SNP analysis of the GFI1-EVI5-RPL5-FAM69 risk locus for multiple sclerosis


GET Evidence
rs6680578
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.570312
summary