rs794728594

Orientation

plus

Stabilized

plus

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

Make rs794728594(A;A)

Make rs794728594(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

156135247

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs794728594
dbSNP (classic)	rs794728594
ClinGen	rs794728594
ebi	rs794728594
HLI	rs794728594
Exac	rs794728594
Gnomad	rs794728594
Varsome	rs794728594
LitVar	rs794728594
Map	rs794728594
PheGenI	rs794728594
Biobank	rs794728594
1000 genomes	rs794728594
hgdp	rs794728594
ensembl	rs794728594
geneview	rs794728594
scholar	rs794728594
google	rs794728594
pharmgkb	rs794728594
gwascentral	rs794728594
openSNP	rs794728594
23andMe	rs794728594
SNPshot	rs794728594
SNPdbe	rs794728594
MSV3d	rs794728594
GWAS Ctlg	rs794728594

Max Magnitude

0

ClinVar
Risk	rs794728594(A;A)
Alt	rs794728594(A;A)
Reference	Rs794728594(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	LMNA
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.156105038G>A
CLNSRC
CLNACC	RCV000182365.2,