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rs6140791

From SNPedia

Orientationplus
Make rs6140791(C;C)
Make rs6140791(C;G)
Make rs6140791(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome20
Position8906576
is asnp
is mentioned by
dbSNPrs6140791
ebirs6140791
HLIrs6140791
Exacrs6140791
Varsomers6140791
Maprs6140791
PheGenIrs6140791
hapmaprs6140791
1000 genomesrs6140791
hgdprs6140791
ensemblrs6140791
gopubmedrs6140791
geneviewrs6140791
scholarrs6140791
googlers6140791
pharmgkbrs6140791
gwascentralrs6140791
openSNPrs6140791
23andMers6140791
23andMe allrs6140791
SNP Nexus

SNPshotrs6140791
SNPdbers6140791
MSV3drs6140791
GWAS Ctlgrs6140791
Max Magnitude
? (C;C) (C;G) (G;G) 28
[PMID 26434682OA-icon.png] Genetic variants in PLCB4/PLCB1 as susceptibility loci for coronary artery aneurysm formation in Kawasaki disease in Han Chinese in Taiwan