rs794728596

Orientation

plus

Stabilized

plus

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

Make rs794728596(G;T)

Make rs794728596(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

156137186

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs794728596
dbSNP (classic)	rs794728596
ClinGen	rs794728596
ebi	rs794728596
HLI	rs794728596
Exac	rs794728596
Gnomad	rs794728596
Varsome	rs794728596
LitVar	rs794728596
Map	rs794728596
PheGenI	rs794728596
Biobank	rs794728596
1000 genomes	rs794728596
hgdp	rs794728596
ensembl	rs794728596
geneview	rs794728596
scholar	rs794728596
google	rs794728596
pharmgkb	rs794728596
gwascentral	rs794728596
openSNP	rs794728596
23andMe	rs794728596
SNPshot	rs794728596
SNPdbe	rs794728596
MSV3d	rs794728596
GWAS Ctlg	rs794728596

Max Magnitude

0

ClinVar
Risk	rs794728596(T;T)
Alt	rs794728596(T;T)
Reference	Rs794728596(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	LMNA
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.156106977G>T
CLNSRC
CLNACC	RCV000182371.2,