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rs2602397

From SNPedia

Merged intors1597944
Orientationplus
Stabilizedplus
Make rs2602397(C;C)
Make rs2602397(C;T)
Make rs2602397(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position233595452
is asnp
is mentioned by
dbSNPrs2602397
ebirs2602397
HLIrs2602397
Exacrs2602397
Varsomers2602397
Maprs2602397
PheGenIrs2602397
hapmaprs2602397
1000 genomesrs2602397
hgdprs2602397
ensemblrs2602397
gopubmedrs2602397
geneviewrs2602397
scholarrs2602397
googlers2602397
pharmgkbrs2602397
gwascentralrs2602397
openSNPrs2602397
23andMers2602397
23andMe allrs2602397
SNP Nexus

SNPshotrs2602397
SNPdbers2602397
MSV3drs2602397
GWAS Ctlgrs2602397
StatusMerged into rs1597944
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 0.000004
Odds Ratio NR NR