rs56771886

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;T)	6.2	Dilated cardiomyopathy
(I;I)	0
(T;T)	0	common in clinvar

Make rs56771886(-;-)

Reference

GRCh38 38.1/141

Chromosome

1

Position

156135923

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs56771886
dbSNP (classic)	rs56771886
ClinGen	rs56771886
ebi	rs56771886
HLI	rs56771886
Exac	rs56771886
Gnomad	rs56771886
Varsome	rs56771886
LitVar	rs56771886
Map	rs56771886
PheGenI	rs56771886
Biobank	rs56771886
1000 genomes	rs56771886
hgdp	rs56771886
ensembl	rs56771886
geneview	rs56771886
scholar	rs56771886
google	rs56771886
pharmgkb	rs56771886
gwascentral	rs56771886
openSNP	rs56771886
23andMe	rs56771886
SNPshot	rs56771886
SNPdbe	rs56771886
MSV3d	rs56771886
GWAS Ctlg	rs56771886

Max Magnitude

6.2

ClinVar
Risk	rs56771886(-;-)
Alt	rs56771886(-;-)
Reference	Rs56771886(T;T)
Significance	Pathogenic
Disease	Dilated cardiomyopathy 1A Benign scapuloperoneal muscular dystrophy with cardiomyopathy not provided
Variation	info
Gene	LMNA
CLNDBN	Dilated cardiomyopathy 1A Benign scapuloperoneal muscular dystrophy with cardiomyopathy not provided
Reversed	0
HGVS	NC_000001.10:g.156105714delT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000015581.22, RCV000015582.26, RCV000057492.1,