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rs137852764

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137852764(A;G)
Make rs137852764(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position19188211
GeneCSRP3
is asnp
is mentioned by
dbSNPrs137852764
ebirs137852764
HLIrs137852764
Exacrs137852764
Varsomers137852764
Maprs137852764
PheGenIrs137852764
hapmaprs137852764
1000 genomesrs137852764
hgdprs137852764
ensemblrs137852764
gopubmedrs137852764
geneviewrs137852764
scholarrs137852764
googlers137852764
pharmgkbrs137852764
gwascentralrs137852764
openSNPrs137852764
23andMers137852764
23andMe allrs137852764
SNP Nexus

SNPshotrs137852764
SNPdbers137852764
MSV3drs137852764
GWAS Ctlgrs137852764
Max Magnitude0
OMIM600824
Desc
Variant0005
Relatedalso
ClinVar
Risk rs137852764(G;G)
Alt rs137852764(G;G)
Reference rs137852764(A;A)
Significance Pathogenic
Disease Dilated cardiomyopathy 1M Familial hypertrophic cardiomyopathy 12
Variation info
Gene CSRP3
CLNDBN Dilated cardiomyopathy 1M Familial hypertrophic cardiomyopathy 12
Reversed 1
HGVS NC_000011.9:g.19209758T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000009325.3, RCV000196843.1,