rs794728613

Orientation

plus

Stabilized

plus

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

Make rs794728613(A;A)

Make rs794728613(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

156136941

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs794728613
dbSNP (classic)	rs794728613
ClinGen	rs794728613
ebi	rs794728613
HLI	rs794728613
Exac	rs794728613
Gnomad	rs794728613
Varsome	rs794728613
LitVar	rs794728613
Map	rs794728613
PheGenI	rs794728613
Biobank	rs794728613
1000 genomes	rs794728613
hgdp	rs794728613
ensembl	rs794728613
geneview	rs794728613
scholar	rs794728613
google	rs794728613
pharmgkb	rs794728613
gwascentral	rs794728613
openSNP	rs794728613
23andMe	rs794728613
SNPshot	rs794728613
SNPdbe	rs794728613
MSV3d	rs794728613
GWAS Ctlg	rs794728613

Max Magnitude

0

ClinVar
Risk	rs794728613(A;A)
Alt	rs794728613(A;A)
Reference	Rs794728613(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	LMNA
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.156106732G>A
CLNSRC
CLNACC	RCV000182396.2,