rs553016

Orientation

minus

Stabilized

minus

Make rs553016(A;A)

Make rs553016(A;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

156137072

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs553016
dbSNP (classic)	rs553016
ClinGen	rs553016
ebi	rs553016
HLI	rs553016
Exac	rs553016
Gnomad	rs553016
Varsome	rs553016
LitVar	rs553016
Map	rs553016
PheGenI	rs553016
Biobank	rs553016
1000 genomes	rs553016
hgdp	rs553016
ensembl	rs553016
geneview	rs553016
scholar	rs553016
google	rs553016
pharmgkb	rs553016
gwascentral	rs553016
openSNP	rs553016
23andMe	rs553016
SNPshot	rs553016
SNPdbe	rs553016
MSV3d	rs553016
GWAS Ctlg	rs553016

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

[PMID 24831476] [Association between LMNA mutation and familial and idiopathic dilated cardiomyopathy patients in Xinjiang]

ClinVar
Risk	rs553016(A;A)
Alt	rs553016(A;A)
Reference	Rs553016(G;G)
Significance	Non-pathogenic
Disease	not provided not specified
Variation	info
Gene	LMNA
CLNDBN	not provided not specified
Reversed	1
HGVS	NC_000001.10:g.156106863C>T
CLNSRC	ClinVar Epithelial Biology
CLNACC	RCV000057308.1, RCV000243967.1,