rs111569862

Orientation

plus

Stabilized

plus

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

Make rs111569862(C;C)

Make rs111569862(C;G)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

156137653

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs111569862
dbSNP (classic)	rs111569862
ClinGen	rs111569862
ebi	rs111569862
HLI	rs111569862
Exac	rs111569862
Gnomad	rs111569862
Varsome	rs111569862
LitVar	rs111569862
Map	rs111569862
PheGenI	rs111569862
Biobank	rs111569862
1000 genomes	rs111569862
hgdp	rs111569862
ensembl	rs111569862
geneview	rs111569862
scholar	rs111569862
google	rs111569862
pharmgkb	rs111569862
gwascentral	rs111569862
openSNP	rs111569862
23andMe	rs111569862
SNPshot	rs111569862
SNPdbe	rs111569862
MSV3d	rs111569862
GWAS Ctlg	rs111569862

Max Magnitude

0

ClinVar
Risk	rs111569862(A;A) rs111569862(C;C)
Alt	rs111569862(A;A) rs111569862(C;C)
Reference	Rs111569862(G;G)
Significance	Pathogenic
Disease	Primary dilated cardiomyopathy not provided Limb-girdle muscular dystrophy
Variation	info
Gene	LMNA
CLNDBN	Primary dilated cardiomyopathy not provided Limb-girdle muscular dystrophy, type 1B
Reversed	0
HGVS	NC_000001.10:g.156107444G>A
CLNSRC
CLNACC	RCV000156608.1, RCV000182373.1, RCV000355258.1,