rs368386019

Orientation

plus

Stabilized

plus

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

Make rs368386019(A;A)

Make rs368386019(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

156138720

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs368386019
dbSNP (classic)	rs368386019
ClinGen	rs368386019
ebi	rs368386019
HLI	rs368386019
Exac	rs368386019
Gnomad	rs368386019
Varsome	rs368386019
LitVar	rs368386019
Map	rs368386019
PheGenI	rs368386019
Biobank	rs368386019
1000 genomes	rs368386019
hgdp	rs368386019
ensembl	rs368386019
geneview	rs368386019
scholar	rs368386019
google	rs368386019
pharmgkb	rs368386019
gwascentral	rs368386019
openSNP	rs368386019
23andMe	rs368386019
SNPshot	rs368386019
SNPdbe	rs368386019
MSV3d	rs368386019
GWAS Ctlg	rs368386019

Max Magnitude

0

ClinVar
Risk	rs368386019(A;A)
Alt	rs368386019(A;A)
Reference	Rs368386019(G;G)
Significance	Probable-non-pathogenic
Disease	Congenital muscular dystrophy not specified Charcot-Marie-Tooth disease Cardiovascular phenotype
Variation	info
Gene	LMNA
CLNDBN	Congenital muscular dystrophy not specified Charcot-Marie-Tooth disease, type 2 Cardiovascular phenotype
Reversed	0
HGVS	NC_000001.10:g.156108511G>A
CLNSRC
CLNACC	RCV000148599.1, RCV000182377.4, RCV000231962.1, RCV000245708.1,