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rs137852765

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137852765(A;C)
Make rs137852765(C;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position19188281
GeneCSRP3
is asnp
is mentioned by
dbSNPrs137852765
ebirs137852765
HLIrs137852765
Exacrs137852765
Varsomers137852765
Maprs137852765
PheGenIrs137852765
hapmaprs137852765
1000 genomesrs137852765
hgdprs137852765
ensemblrs137852765
gopubmedrs137852765
geneviewrs137852765
scholarrs137852765
googlers137852765
pharmgkbrs137852765
gwascentralrs137852765
openSNPrs137852765
23andMers137852765
23andMe allrs137852765
SNP Nexus

SNPshotrs137852765
SNPdbers137852765
MSV3drs137852765
GWAS Ctlgrs137852765
Max Magnitude0
OMIM600824
Desc
Variant0006
Relatedalso
ClinVar
Risk rs137852765(C;C)
Alt rs137852765(C;C)
Reference rs137852765(A;A)
Significance Pathogenic
Disease Familial hypertrophic cardiomyopathy 12 Primary dilated cardiomyopathy not provided
Variation info
Gene CSRP3
CLNDBN Familial hypertrophic cardiomyopathy 12 Primary dilated cardiomyopathy not provided
Reversed 1
HGVS NC_000011.9:g.19209828T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000009326.3, RCV000150369.2, RCV000183335.1,