Have questions? Visit https://www.reddit.com/r/SNPedia

rs193922668

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ATT;ATT) 0 common in clinvar
Make rs193922668(-;-)
Make rs193922668(-;ATT)
ReferenceGRCh38 38.1/141
Chromosome6
Position7568554
GeneDSP
is asnp
is mentioned by
dbSNPrs193922668
ebirs193922668
HLIrs193922668
Exacrs193922668
Varsomers193922668
Maprs193922668
PheGenIrs193922668
hapmaprs193922668
1000 genomesrs193922668
hgdprs193922668
ensemblrs193922668
gopubmedrs193922668
geneviewrs193922668
scholarrs193922668
googlers193922668
pharmgkbrs193922668
gwascentralrs193922668
openSNPrs193922668
23andMers193922668
23andMe allrs193922668
SNP Nexus

SNPshotrs193922668
SNPdbers193922668
MSV3drs193922668
GWAS Ctlgrs193922668
Max Magnitude0
ClinVar
Risk rs193922668(;)
Alt rs193922668(;)
Reference rs193922668(ATT;ATT)
Significance Probable-Pathogenic
Disease Cardiomyopathy
Variation info
Gene DSP
CLNDBN Cardiomyopathy
Reversed 0
HGVS NC_000006.11:g.7568787_7568789delATT
CLNSRC ClinVar
CLNACC RCV000029676.1,