rs794728591

Orientation

plus

Stabilized

plus

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

Make rs794728591(C;T)

Make rs794728591(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

156134811

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs794728591
dbSNP (classic)	rs794728591
ClinGen	rs794728591
ebi	rs794728591
HLI	rs794728591
Exac	rs794728591
Gnomad	rs794728591
Varsome	rs794728591
LitVar	rs794728591
Map	rs794728591
PheGenI	rs794728591
Biobank	rs794728591
1000 genomes	rs794728591
hgdp	rs794728591
ensembl	rs794728591
geneview	rs794728591
scholar	rs794728591
google	rs794728591
pharmgkb	rs794728591
gwascentral	rs794728591
openSNP	rs794728591
23andMe	rs794728591
SNPshot	rs794728591
SNPdbe	rs794728591
MSV3d	rs794728591
GWAS Ctlg	rs794728591

Max Magnitude

0

ClinVar
Risk	rs794728591(T;T)
Alt	rs794728591(T;T)
Reference	Rs794728591(C;C)
Significance	Probable-Pathogenic
Disease	not specified Primary dilated cardiomyopathy Cardiovascular phenotype
Variation	info
Gene	LMNA
CLNDBN	not specified Primary dilated cardiomyopathy Cardiovascular phenotype
Reversed	0
HGVS	NC_000001.10:g.156104602C>T
CLNSRC
CLNACC	RCV000182360.5, RCV000208531.1, RCV000241819.1,