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Rs7577363

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Orientationplus
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
PheGenIrs7577363
nextbiors7577363
hapmaprs7577363
1000 genomesrs7577363
hgdprs7577363
ensemblrs7577363
gopubmedrs7577363
geneviewrs7577363
scholarrs7577363
googlers7577363
pharmgkbrs7577363
gwascentralrs7577363
openSNPrs7577363
23andMers7577363
23andMe allrs7577363
SNP Nexus

SNPshotrs7577363
SNPdbers7577363
MSV3drs7577363
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]



GET Evidence
rs7577363
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.0703125
summary



[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.