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rs2039485

From SNPedia

Orientationplus
Stabilizedplus
Make rs2039485(C;C)
Make rs2039485(C;T)
Make rs2039485(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position31884044
is asnp
is mentioned by
dbSNPrs2039485
ebirs2039485
HLIrs2039485
Exacrs2039485
Varsomers2039485
Maprs2039485
PheGenIrs2039485
hapmaprs2039485
1000 genomesrs2039485
hgdprs2039485
ensemblrs2039485
gopubmedrs2039485
geneviewrs2039485
scholarrs2039485
googlers2039485
pharmgkbrs2039485
gwascentralrs2039485
openSNPrs2039485
23andMers2039485
23andMe allrs2039485
SNP Nexus

SNPshotrs2039485
SNPdbers2039485
MSV3drs2039485
GWAS Ctlgrs2039485
GMAF0.2576
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19010793OA-icon.png]
Trait Brain lesion load
Title Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis
Risk Allele
P-val 0.000006
Odds Ratio NR NR



GET Evidence
rs2039485
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.195312
summary