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rs193922671

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs193922671(C;G)
Make rs193922671(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position7585226
GeneDSP
is asnp
is mentioned by
dbSNPrs193922671
ebirs193922671
HLIrs193922671
Exacrs193922671
Varsomers193922671
Maprs193922671
PheGenIrs193922671
hapmaprs193922671
1000 genomesrs193922671
hgdprs193922671
ensemblrs193922671
gopubmedrs193922671
geneviewrs193922671
scholarrs193922671
googlers193922671
pharmgkbrs193922671
gwascentralrs193922671
openSNPrs193922671
23andMers193922671
23andMe allrs193922671
SNP Nexus

SNPshotrs193922671
SNPdbers193922671
MSV3drs193922671
GWAS Ctlgrs193922671
Max Magnitude0
ClinVar
Risk rs193922671(G;G)
Alt rs193922671(G;G)
Reference rs193922671(C;C)
Significance Probable-Pathogenic
Disease Cardiomyopathy
Variation info
Gene DSP
CLNDBN Cardiomyopathy
Reversed 0
HGVS NC_000006.11:g.7585459C>G
CLNSRC ClinVar LabCorp
CLNACC RCV000029683.1,