rs794728586

Orientation

plus

Stabilized

plus

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

Make rs794728586(C;C)

Make rs794728586(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

156115170

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs794728586
dbSNP (classic)	rs794728586
ClinGen	rs794728586
ebi	rs794728586
HLI	rs794728586
Exac	rs794728586
Gnomad	rs794728586
Varsome	rs794728586
LitVar	rs794728586
Map	rs794728586
PheGenI	rs794728586
Biobank	rs794728586
1000 genomes	rs794728586
hgdp	rs794728586
ensembl	rs794728586
geneview	rs794728586
scholar	rs794728586
google	rs794728586
pharmgkb	rs794728586
gwascentral	rs794728586
openSNP	rs794728586
23andMe	rs794728586
SNPshot	rs794728586
SNPdbe	rs794728586
MSV3d	rs794728586
GWAS Ctlg	rs794728586

Max Magnitude

0

ClinVar
Risk	rs794728586(C;C)
Alt	rs794728586(C;C)
Reference	Rs794728586(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	LMNA
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.156084961G>C
CLNSRC
CLNACC	RCV000182351.1,