rs794728612

Orientation

plus

Stabilized

plus

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

Make rs794728612(CG;TC)

Make rs794728612(TC;TC)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

156137756

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs794728612
dbSNP (classic)	rs794728612
ClinGen	rs794728612
ebi	rs794728612
HLI	rs794728612
Exac	rs794728612
Gnomad	rs794728612
Varsome	rs794728612
LitVar	rs794728612
Map	rs794728612
PheGenI	rs794728612
Biobank	rs794728612
1000 genomes	rs794728612
hgdp	rs794728612
ensembl	rs794728612
geneview	rs794728612
scholar	rs794728612
google	rs794728612
pharmgkb	rs794728612
gwascentral	rs794728612
openSNP	rs794728612
23andMe	rs794728612
SNPshot	rs794728612
SNPdbe	rs794728612
MSV3d	rs794728612
GWAS Ctlg	rs794728612

Max Magnitude

0

ClinVar
Risk	rs794728612(TC;TC)
Alt	rs794728612(TC;TC)
Reference	Rs794728612(CG;CG)
Significance	Pathogenic
Disease	not provided Cardiovascular phenotype not specified
Variation	info
Gene	LMNA
CLNDBN	not provided Cardiovascular phenotype not specified
Reversed	0
HGVS	NC_000001.10:g.156107547_156107548delCGinsTC
CLNSRC
CLNACC	RCV000182393.1, RCV000249124.1, RCV000362173.1,