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rs12590667

From SNPedia

Orientationplus
Stabilizedplus
Make rs12590667(C;C)
Make rs12590667(C;T)
Make rs12590667(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position106779223
GeneIGH@
is asnp
is mentioned by
dbSNPrs12590667
ebirs12590667
HLIrs12590667
Exacrs12590667
Varsomers12590667
Maprs12590667
PheGenIrs12590667
hapmaprs12590667
1000 genomesrs12590667
hgdprs12590667
ensemblrs12590667
gopubmedrs12590667
geneviewrs12590667
scholarrs12590667
googlers12590667
pharmgkbrs12590667
gwascentralrs12590667
openSNPrs12590667
23andMers12590667
23andMe allrs12590667
SNP Nexus

SNPshotrs12590667
SNPdbers12590667
MSV3drs12590667
GWAS Ctlgrs12590667
GMAF0.32
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 21326860OA-icon.png] Identification of novel susceptibility Loci for kawasaki disease in a Han chinese population by a genome-wide association study