rs28928903

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;G)	6.2	Dilated cardiomyopathy
(G;G)	0	common in clinvar

Make rs28928903(C;C)

Reference

GRCh38 38.1/141

Chromosome

1

Position

156115087

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs28928903
dbSNP (classic)	rs28928903
ClinGen	rs28928903
ebi	rs28928903
HLI	rs28928903
Exac	rs28928903
Gnomad	rs28928903
Varsome	rs28928903
LitVar	rs28928903
Map	rs28928903
PheGenI	rs28928903
Biobank	rs28928903
1000 genomes	rs28928903
hgdp	rs28928903
ensembl	rs28928903
geneview	rs28928903
scholar	rs28928903
google	rs28928903
pharmgkb	rs28928903
gwascentral	rs28928903
openSNP	rs28928903
23andMe	rs28928903
SNPshot	rs28928903
SNPdbe	rs28928903
MSV3d	rs28928903
GWAS Ctlg	rs28928903

Max Magnitude

6.2

OMIM	150330
Desc	WERNER SYNDROME, ATYPICAL
Variant	0030
Related	also

ClinVar
Risk	rs28928903(C;C)
Alt	rs28928903(C;C)
Reference	Rs28928903(G;G)
Significance	Pathogenic
Disease	Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome not provided
Variation	info
Gene	LMNA
CLNDBN	Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome not provided
Reversed	0
HGVS	NC_000001.10:g.156084878G>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000015600.24, RCV000057349.1,