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rs1003199

From SNPedia

Orientationplus
Stabilizedplus
Make rs1003199(C;C)
Make rs1003199(C;T)
Make rs1003199(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position159328558
GeneIL12B
is asnp
is mentioned by
dbSNPrs1003199
ebirs1003199
HLIrs1003199
Exacrs1003199
Varsomers1003199
Maprs1003199
PheGenIrs1003199
hapmaprs1003199
1000 genomesrs1003199
hgdprs1003199
ensemblrs1003199
gopubmedrs1003199
geneviewrs1003199
scholarrs1003199
googlers1003199
pharmgkbrs1003199
gwascentralrs1003199
openSNPrs1003199
23andMers1003199
23andMe allrs1003199
SNP Nexus

SNPshotrs1003199
SNPdbers1003199
MSV3drs1003199
GWAS Ctlgrs1003199
GMAF0.3669
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 23164360OA-icon.png] Association of IL12B polymorphisms with susceptibility to Graves ophthalmopathy in a Taiwan Chinese population