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rs142019584

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs142019584(A;A)
Make rs142019584(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position19182719
GeneCSRP3
is asnp
is mentioned by
dbSNPrs142019584
ebirs142019584
HLIrs142019584
Exacrs142019584
Varsomers142019584
Maprs142019584
PheGenIrs142019584
hapmaprs142019584
1000 genomesrs142019584
hgdprs142019584
ensemblrs142019584
gopubmedrs142019584
geneviewrs142019584
scholarrs142019584
googlers142019584
pharmgkbrs142019584
gwascentralrs142019584
openSNPrs142019584
23andMers142019584
23andMe allrs142019584
SNP Nexus

SNPshotrs142019584
SNPdbers142019584
MSV3drs142019584
GWAS Ctlgrs142019584
Max Magnitude0
ClinVar
Risk rs142019584(A;A)
Alt rs142019584(A;A)
Reference rs142019584(G;G)
Significance Probable-Pathogenic
Disease not specified Familial hypertrophic cardiomyopathy 12 Dilated cardiomyopathy 1M
Variation info
Gene CSRP3
CLNDBN not specified Familial hypertrophic cardiomyopathy 12 Dilated cardiomyopathy 1M
Reversed 0
HGVS NC_000011.9:g.19204266G>A
CLNSRC
CLNACC RCV000150366.1, RCV000201497.1, RCV000231901.1,