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rs1597944

From SNPedia

Orientationplus
Stabilizedplus
Make rs1597944(C;C)
Make rs1597944(C;T)
Make rs1597944(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position233595452
is asnp
is mentioned by
dbSNPrs1597944
ebirs1597944
HLIrs1597944
Exacrs1597944
Varsomers1597944
Maprs1597944
PheGenIrs1597944
hapmaprs1597944
1000 genomesrs1597944
hgdprs1597944
ensemblrs1597944
gopubmedrs1597944
geneviewrs1597944
scholarrs1597944
googlers1597944
pharmgkbrs1597944
gwascentralrs1597944
openSNPrs1597944
23andMers1597944
23andMe allrs1597944
SNP Nexus

SNPshotrs1597944
SNPdbers1597944
MSV3drs1597944
GWAS Ctlgrs1597944
Merged fromRs2602397
GMAF0.4394
Max Magnitude
? (C;C) (C;T) (T;T) 28
? (C;C) (C;T) (T;T)
[PMID 19010793OA-icon.png] Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.