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rs996343

From SNPedia

Orientationminus
Stabilizedminus
Make rs996343(C;C)
Make rs996343(C;T)
Make rs996343(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position145321424
is asnp
is mentioned by
dbSNPrs996343
ebirs996343
HLIrs996343
Exacrs996343
Varsomers996343
Maprs996343
PheGenIrs996343
hapmaprs996343
1000 genomesrs996343
hgdprs996343
ensemblrs996343
gopubmedrs996343
geneviewrs996343
scholarrs996343
googlers996343
pharmgkbrs996343
gwascentralrs996343
openSNPrs996343
23andMers996343
23andMe allrs996343
SNP Nexus

SNPshotrs996343
SNPdbers996343
MSV3drs996343
GWAS Ctlgrs996343
GMAF0.4908
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 22457343] A genome-wide association study in progressive multiple sclerosis