rs56851164

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(T;T)	0	common in clinvar

Make rs56851164(A;A)

Make rs56851164(A;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

156135940

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs56851164
dbSNP (classic)	rs56851164
ClinGen	rs56851164
ebi	rs56851164
HLI	rs56851164
Exac	rs56851164
Gnomad	rs56851164
Varsome	rs56851164
LitVar	rs56851164
Map	rs56851164
PheGenI	rs56851164
Biobank	rs56851164
1000 genomes	rs56851164
hgdp	rs56851164
ensembl	rs56851164
geneview	rs56851164
scholar	rs56851164
google	rs56851164
pharmgkb	rs56851164
gwascentral	rs56851164
openSNP	rs56851164
23andMe	rs56851164
SNPshot	rs56851164
SNPdbe	rs56851164
MSV3d	rs56851164
GWAS Ctlg	rs56851164

Max Magnitude

0

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, RCV000212504.2,