rs267607573

Orientation

plus

Stabilized

plus

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

Make rs267607573(C;T)

Make rs267607573(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

156134865

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs267607573
dbSNP (classic)	rs267607573
ClinGen	rs267607573
ebi	rs267607573
HLI	rs267607573
Exac	rs267607573
Gnomad	rs267607573
Varsome	rs267607573
LitVar	rs267607573
Map	rs267607573
PheGenI	rs267607573
Biobank	rs267607573
1000 genomes	rs267607573
hgdp	rs267607573
ensembl	rs267607573
geneview	rs267607573
scholar	rs267607573
google	rs267607573
pharmgkb	rs267607573
gwascentral	rs267607573
openSNP	rs267607573
23andMe	rs267607573
SNPshot	rs267607573
SNPdbe	rs267607573
MSV3d	rs267607573
GWAS Ctlg	rs267607573

Max Magnitude

0

ClinVar
Risk	rs267607573(T;T)
Alt	rs267607573(T;T)
Reference	Rs267607573(C;C)
Significance	Probable-Pathogenic
Disease	Primary dilated cardiomyopathy not provided
Variation	info
Gene	LMNA
CLNDBN	Primary dilated cardiomyopathy not provided
Reversed	0
HGVS	NC_000001.10:g.156104656C>T
CLNSRC	ClinVar Epithelial Biology
CLNACC	RCV000041360.2, RCV000057446.1,