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rs337718

From SNPedia

Orientationplus
Stabilizedplus
Make rs337718(C;C)
Make rs337718(C;T)
Make rs337718(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position72107043
is asnp
is mentioned by
dbSNPrs337718
ebirs337718
HLIrs337718
Exacrs337718
Varsomers337718
Maprs337718
PheGenIrs337718
hapmaprs337718
1000 genomesrs337718
hgdprs337718
ensemblrs337718
gopubmedrs337718
geneviewrs337718
scholarrs337718
googlers337718
pharmgkbrs337718
gwascentralrs337718
openSNPrs337718
23andMers337718
23andMe allrs337718
SNP Nexus

SNPshotrs337718
SNPdbers337718
MSV3drs337718
GWAS Ctlgrs337718
GMAF0.3352
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 0.000009
Odds Ratio NR NR



GET Evidence
rs337718
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.650794
summary