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rs193922667

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922667(A;A)
Make rs193922667(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position19186265
GeneCSRP3
is asnp
is mentioned by
dbSNPrs193922667
ebirs193922667
HLIrs193922667
Exacrs193922667
Varsomers193922667
Maprs193922667
PheGenIrs193922667
hapmaprs193922667
1000 genomesrs193922667
hgdprs193922667
ensemblrs193922667
gopubmedrs193922667
geneviewrs193922667
scholarrs193922667
googlers193922667
pharmgkbrs193922667
gwascentralrs193922667
openSNPrs193922667
23andMers193922667
23andMe allrs193922667
SNP Nexus

SNPshotrs193922667
SNPdbers193922667
MSV3drs193922667
GWAS Ctlgrs193922667
Max Magnitude0
ClinVar
Risk rs193922667(A;A)
Alt rs193922667(A;A)
Reference rs193922667(G;G)
Significance Probable-Pathogenic
Disease Cardiomyopathy
Variation info
Gene CSRP3
CLNDBN Cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.19207812C>T
CLNSRC ClinVar LabCorp
CLNACC RCV000029622.1,