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rs7577363

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) >1.37x risk
(A;G) 1.37x risk
(C;C) 0
(G;G) 0 common
ReferenceGRCh38 38.1/141
Chromosome2
Position29653477
GeneALK
is asnp
is mentioned by
dbSNPrs7577363
dbSNP (classic)rs7577363
ClinGenrs7577363
ebirs7577363
HLIrs7577363
Exacrs7577363
Gnomadrs7577363
Varsomers7577363
LitVarrs7577363
Maprs7577363
PheGenIrs7577363
Biobankrs7577363
1000 genomesrs7577363
hgdprs7577363
ensemblrs7577363
geneviewrs7577363
scholarrs7577363
googlers7577363
pharmgkbrs7577363
gwascentralrs7577363
openSNPrs7577363
23andMers7577363
SNPshotrs7577363
SNPdbers7577363
MSV3drs7577363
GWAS Ctlgrs7577363
GMAF0.07668
Max Magnitude0
? (A;A) (A;G) (G;G) 28


rs7577363 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 1.37 (CI 1.17-1.61). [PMID 17660530]




[PMID 22492128] Association of SNPs rs6498169 and rs10984447 with multiple sclerosis in Saudi patients: a model of the usefulness of familial aggregates in identifying genetic linkage in a multifactorial disease.