rs267607539

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;G)	6.2	Dilated cardiomyopathy
(C;G)	6.4	Emery-Dreifuss Muscular Dystrophy
(G;G)	0	common in clinvar

Make rs267607539(C;C)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

156137237

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs267607539
dbSNP (classic)	rs267607539
ClinGen	rs267607539
ebi	rs267607539
HLI	rs267607539
Exac	rs267607539
Gnomad	rs267607539
Varsome	rs267607539
LitVar	rs267607539
Map	rs267607539
PheGenI	rs267607539
Biobank	rs267607539
1000 genomes	rs267607539
hgdp	rs267607539
ensembl	rs267607539
geneview	rs267607539
scholar	rs267607539
google	rs267607539
pharmgkb	rs267607539
gwascentral	rs267607539
openSNP	rs267607539
23andMe	rs267607539
SNPshot	rs267607539
SNPdbe	rs267607539
MSV3d	rs267607539
GWAS Ctlg	rs267607539

Max Magnitude

6.4

ClinVar
Risk	rs267607539(C;C)
Alt	rs267607539(C;C)
Reference	Rs267607539(G;G)
Significance	Pathogenic
Disease	Limb-girdle muscular dystrophy not provided
Variation	info
Gene	LMNA
CLNDBN	Limb-girdle muscular dystrophy, type 1B not provided
Reversed	0
HGVS	NC_000001.10:g.156107028G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000015589.26, RCV000057336.1,