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rs56851164

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs56851164(A;A)
Make rs56851164(A;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position156135940
GeneLMNA
is asnp
is mentioned by
dbSNPrs56851164
ebirs56851164
HLIrs56851164
Exacrs56851164
Varsomers56851164
Maprs56851164
PheGenIrs56851164
hapmaprs56851164
1000 genomesrs56851164
hgdprs56851164
ensemblrs56851164
gopubmedrs56851164
geneviewrs56851164
scholarrs56851164
googlers56851164
pharmgkbrs56851164
gwascentralrs56851164
openSNPrs56851164
23andMers56851164
23andMe allrs56851164
SNP Nexus

SNPshotrs56851164
SNPdbers56851164
MSV3drs56851164
GWAS Ctlgrs56851164
Max Magnitude0
ClinVar
Risk rs56851164(A;A)
Alt rs56851164(A;A)
Reference rs56851164(T;T)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy not provided Primary familial hypertrophic cardiomyopathy not specified
Variation info
Gene LMNA
CLNDBN Primary dilated cardiomyopathy not provided Primary familial hypertrophic cardiomyopathy not specified
Reversed 0
HGVS NC_000001.10:g.156105731T>A
CLNSRC ClinVar Epithelial Biology
CLNACC RCV000041383.2, RCV000057494.3, RCV000208012.1, RCV000212504.1,