rs794728601

Orientation

plus

Stabilized

plus

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

Make rs794728601(C;C)

Make rs794728601(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

156115097

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs794728601
dbSNP (classic)	rs794728601
ClinGen	rs794728601
ebi	rs794728601
HLI	rs794728601
Exac	rs794728601
Gnomad	rs794728601
Varsome	rs794728601
LitVar	rs794728601
Map	rs794728601
PheGenI	rs794728601
Biobank	rs794728601
1000 genomes	rs794728601
hgdp	rs794728601
ensembl	rs794728601
geneview	rs794728601
scholar	rs794728601
google	rs794728601
pharmgkb	rs794728601
gwascentral	rs794728601
openSNP	rs794728601
23andMe	rs794728601
SNPshot	rs794728601
SNPdbe	rs794728601
MSV3d	rs794728601
GWAS Ctlg	rs794728601

Max Magnitude

0

ClinVar
Risk	rs794728601(C;C)
Alt	rs794728601(C;C)
Reference	Rs794728601(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	LMNA
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.156084888G>C
CLNSRC
CLNACC	RCV000182381.2,