rs267607593

Orientation

plus

Stabilized

plus

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

Make rs267607593(C;C)

Make rs267607593(C;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

156134964

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs267607593
dbSNP (classic)	rs267607593
ClinGen	rs267607593
ebi	rs267607593
HLI	rs267607593
Exac	rs267607593
Gnomad	rs267607593
Varsome	rs267607593
LitVar	rs267607593
Map	rs267607593
PheGenI	rs267607593
Biobank	rs267607593
1000 genomes	rs267607593
hgdp	rs267607593
ensembl	rs267607593
geneview	rs267607593
scholar	rs267607593
google	rs267607593
pharmgkb	rs267607593
gwascentral	rs267607593
openSNP	rs267607593
23andMe	rs267607593
SNPshot	rs267607593
SNPdbe	rs267607593
MSV3d	rs267607593
GWAS Ctlg	rs267607593

Max Magnitude

0

ClinVar
Risk	rs267607593(C;C)
Alt	rs267607593(C;C)
Reference	Rs267607593(T;T)
Significance	Pathogenic
Disease	Primary dilated cardiomyopathy not provided
Variation	info
Gene	LMNA
CLNDBN	Primary dilated cardiomyopathy not provided
Reversed	0
HGVS	NC_000001.10:g.156104755T>C
CLNSRC	ClinVar Epithelial Biology
CLNACC	RCV000041369.2, RCV000057461.3,