rs794728600

Orientation

plus

Stabilized

plus

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

Make rs794728600(C;C)

Make rs794728600(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

156114995

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs794728600
dbSNP (classic)	rs794728600
ClinGen	rs794728600
ebi	rs794728600
HLI	rs794728600
Exac	rs794728600
Gnomad	rs794728600
Varsome	rs794728600
LitVar	rs794728600
Map	rs794728600
PheGenI	rs794728600
Biobank	rs794728600
1000 genomes	rs794728600
hgdp	rs794728600
ensembl	rs794728600
geneview	rs794728600
scholar	rs794728600
google	rs794728600
pharmgkb	rs794728600
gwascentral	rs794728600
openSNP	rs794728600
23andMe	rs794728600
SNPshot	rs794728600
SNPdbe	rs794728600
MSV3d	rs794728600
GWAS Ctlg	rs794728600

Max Magnitude

0

ClinVar
Risk	rs794728600(C;C)
Alt	rs794728600(C;C)
Reference	Rs794728600(T;T)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	LMNA
CLNDBN	not specified
Reversed	0
HGVS	NC_000001.10:g.156084786T>C
CLNSRC
CLNACC	RCV000182380.2,