rs267607554

Orientation

plus

Stabilized

plus

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

Make rs267607554(C;T)

Make rs267607554(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

156135925

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs267607554
dbSNP (classic)	rs267607554
ClinGen	rs267607554
ebi	rs267607554
HLI	rs267607554
Exac	rs267607554
Gnomad	rs267607554
Varsome	rs267607554
LitVar	rs267607554
Map	rs267607554
PheGenI	rs267607554
Biobank	rs267607554
1000 genomes	rs267607554
hgdp	rs267607554
ensembl	rs267607554
geneview	rs267607554
scholar	rs267607554
google	rs267607554
pharmgkb	rs267607554
gwascentral	rs267607554
openSNP	rs267607554
23andMe	rs267607554
SNPshot	rs267607554
SNPdbe	rs267607554
MSV3d	rs267607554
GWAS Ctlg	rs267607554

Max Magnitude

0

ClinVar
Risk	rs267607554(T;T)
Alt	rs267607554(T;T)
Reference	Rs267607554(C;C)
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.156105716C>T
CLNSRC	ClinVar Epithelial Biology
CLNACC	RCV000041382.3, RCV000057493.3,