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rs1557351

From SNPedia

Orientationplus
Stabilizedplus
Make rs1557351(C;C)
Make rs1557351(C;T)
Make rs1557351(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position57085083
is asnp
is mentioned by
dbSNPrs1557351
ebirs1557351
HLIrs1557351
Exacrs1557351
Varsomers1557351
Maprs1557351
PheGenIrs1557351
hapmaprs1557351
1000 genomesrs1557351
hgdprs1557351
ensemblrs1557351
gopubmedrs1557351
geneviewrs1557351
scholarrs1557351
googlers1557351
pharmgkbrs1557351
gwascentralrs1557351
openSNPrs1557351
23andMers1557351
23andMe allrs1557351
SNP Nexus

SNPshotrs1557351
SNPdbers1557351
MSV3drs1557351
GWAS Ctlgrs1557351
GMAF0.3118
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19010793OA-icon.png]
Trait Multiple sclerosis (age of onset)
Title Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis
Risk Allele
P-val 0.000004
Odds Ratio NR NR



GET Evidence
rs1557351
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.296875
summary