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rs651477

From SNPedia

Orientationminus
Stabilizedminus
Make rs651477(A;A)
Make rs651477(A;G)
Make rs651477(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position118638115
is asnp
is mentioned by
dbSNPrs651477
ebirs651477
HLIrs651477
Exacrs651477
Varsomers651477
Maprs651477
PheGenIrs651477
hapmaprs651477
1000 genomesrs651477
hgdprs651477
ensemblrs651477
gopubmedrs651477
geneviewrs651477
scholarrs651477
googlers651477
pharmgkbrs651477
gwascentralrs651477
openSNPrs651477
23andMers651477
23andMe allrs651477
SNP Nexus

SNPshotrs651477
SNPdbers651477
MSV3drs651477
GWAS Ctlgrs651477
GMAF0.242
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19010793OA-icon.png]
Trait Multiple sclerosis
Title Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis
Risk Allele
P-val 0.000007
Odds Ratio 1.38 [NR]



[PMID 20944657] Replication of top markers of a genome-wide association study in multiple sclerosis in Spain.


GET Evidence
rs651477
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.257812
summary