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rs1873668

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs1873668(G;T)
Make rs1873668(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position139326219
is asnp
is mentioned by
dbSNPrs1873668
ebirs1873668
HLIrs1873668
Exacrs1873668
Varsomers1873668
Maprs1873668
PheGenIrs1873668
hapmaprs1873668
1000 genomesrs1873668
hgdprs1873668
ensemblrs1873668
gopubmedrs1873668
geneviewrs1873668
scholarrs1873668
googlers1873668
pharmgkbrs1873668
gwascentralrs1873668
openSNPrs1873668
23andMers1873668
23andMe allrs1873668
SNP Nexus

SNPshotrs1873668
SNPdbers1873668
MSV3drs1873668
GWAS Ctlgrs1873668
GMAF0.0854
Max Magnitude0
? (G;G) (G;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