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rs193922683

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs193922683(C;T)
Make rs193922683(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position21852457
GeneABCC9
is asnp
is mentioned by
dbSNPrs193922683
ebirs193922683
HLIrs193922683
Exacrs193922683
Varsomers193922683
Maprs193922683
PheGenIrs193922683
hapmaprs193922683
1000 genomesrs193922683
hgdprs193922683
ensemblrs193922683
gopubmedrs193922683
geneviewrs193922683
scholarrs193922683
googlers193922683
pharmgkbrs193922683
gwascentralrs193922683
openSNPrs193922683
23andMers193922683
23andMe allrs193922683
SNP Nexus

SNPshotrs193922683
SNPdbers193922683
MSV3drs193922683
GWAS Ctlgrs193922683
Max Magnitude0
ClinVar
Risk rs193922683(T;T)
Alt rs193922683(T;T)
Reference rs193922683(C;C)
Significance Probable-Pathogenic
Disease Cardiomyopathy
Variation info
Gene ABCC9
CLNDBN Cardiomyopathy
Reversed 1
HGVS NC_000012.11:g.22005391G>A
CLNSRC ClinVar
CLNACC RCV000029276.1,