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rs1437898

From SNPedia

Orientationminus
Stabilizedminus
Make rs1437898(G;G)
Make rs1437898(G;T)
Make rs1437898(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position132989057
GeneNCKAP5
is asnp
is mentioned by
dbSNPrs1437898
ebirs1437898
HLIrs1437898
Exacrs1437898
Varsomers1437898
Maprs1437898
PheGenIrs1437898
hapmaprs1437898
1000 genomesrs1437898
hgdprs1437898
ensemblrs1437898
gopubmedrs1437898
geneviewrs1437898
scholarrs1437898
googlers1437898
pharmgkbrs1437898
gwascentralrs1437898
openSNPrs1437898
23andMers1437898
23andMe allrs1437898
SNP Nexus

SNPshotrs1437898
SNPdbers1437898
MSV3drs1437898
GWAS Ctlgrs1437898
GMAF0.4334
Max Magnitude
? (G;G) (G;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 0.000008
Odds Ratio NR NR



GET Evidence
rs1437898
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.546875
summary