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rs11673492

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs11673492(C;T)
Make rs11673492(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position40714624
GeneCOQ8B
is asnp
is mentioned by
dbSNPrs11673492
dbSNP (classic)rs11673492
ClinGenrs11673492
ebirs11673492
HLIrs11673492
Exacrs11673492
Gnomadrs11673492
Varsomers11673492
LitVarrs11673492
Maprs11673492
PheGenIrs11673492
Biobankrs11673492
1000 genomesrs11673492
hgdprs11673492
ensemblrs11673492
geneviewrs11673492
scholarrs11673492
googlers11673492
pharmgkbrs11673492
gwascentralrs11673492
openSNPrs11673492
23andMers11673492
SNPshotrs11673492
SNPdbers11673492
MSV3drs11673492
GWAS Ctlgrs11673492
GMAF0.1267
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 24621571OA-icon.png] Single-Nucleotide Polymorphism rs7251246 in ITPKC Is Associated with Susceptibility and Coronary Artery Lesions in Kawasaki Disease


ClinVar
Risk rs11673492(T;T)
Alt rs11673492(T;T)
Reference Rs11673492(C;C)
Significance Non-pathogenic
Disease not specified
Variation info
Gene COQ8B ADCK4
CLNDBN not specified
Reversed 0
HGVS NC_000019.9:g.41220529C>T
CLNSRC
CLNACC RCV000432894.1,