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rs689732

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs689732(C;G)
Make rs689732(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position153960408
is asnp
is mentioned by
dbSNPrs689732
ebirs689732
HLIrs689732
Exacrs689732
Varsomers689732
Maprs689732
PheGenIrs689732
hapmaprs689732
1000 genomesrs689732
hgdprs689732
ensemblrs689732
gopubmedrs689732
geneviewrs689732
scholarrs689732
googlers689732
pharmgkbrs689732
gwascentralrs689732
openSNPrs689732
23andMers689732
23andMe allrs689732
SNP Nexus

SNPshotrs689732
SNPdbers689732
MSV3drs689732
GWAS Ctlgrs689732
Max Magnitude0
? (C;C) (C;G) (G;G) 28
OMIM612595
DescMULTIPLE SCLEROSIS, SUSCEPTIBILITY TO, 3; MS3
Variant
Relatedalso