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rs193922669

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922669(A;A)
Make rs193922669(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position7582817
GeneDSP
is asnp
is mentioned by
dbSNPrs193922669
ebirs193922669
HLIrs193922669
Exacrs193922669
Varsomers193922669
Maprs193922669
PheGenIrs193922669
hapmaprs193922669
1000 genomesrs193922669
hgdprs193922669
ensemblrs193922669
gopubmedrs193922669
geneviewrs193922669
scholarrs193922669
googlers193922669
pharmgkbrs193922669
gwascentralrs193922669
openSNPrs193922669
23andMers193922669
23andMe allrs193922669
SNP Nexus

SNPshotrs193922669
SNPdbers193922669
MSV3drs193922669
GWAS Ctlgrs193922669
Max Magnitude0
ClinVar
Risk rs193922669(A;A)
Alt rs193922669(A;A)
Reference rs193922669(G;G)
Significance Probable-Pathogenic
Disease Arrhythmogenic right ventricular cardiomyopathy
Variation info
Gene DSP
CLNDBN Arrhythmogenic right ventricular cardiomyopathy
Reversed 0
HGVS NC_000006.11:g.7583050G>A
CLNSRC ClinVar LabCorp
CLNACC RCV000029681.1,