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rs1478091

From SNPedia

Orientationplus
Stabilizedplus
Make rs1478091(C;C)
Make rs1478091(C;T)
Make rs1478091(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position130869346
is asnp
is mentioned by
dbSNPrs1478091
ebirs1478091
HLIrs1478091
Exacrs1478091
Varsomers1478091
Maprs1478091
PheGenIrs1478091
hapmaprs1478091
1000 genomesrs1478091
hgdprs1478091
ensemblrs1478091
gopubmedrs1478091
geneviewrs1478091
scholarrs1478091
googlers1478091
pharmgkbrs1478091
gwascentralrs1478091
openSNPrs1478091
23andMers1478091
23andMe allrs1478091
SNP Nexus

SNPshotrs1478091
SNPdbers1478091
MSV3drs1478091
GWAS Ctlgrs1478091
GMAF0.1671
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19010793OA-icon.png]
Trait Multiple sclerosis (severity)
Title Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis
Risk Allele
P-val 0.000002
Odds Ratio NR NR



GET Evidence
rs1478091
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.757812
summary