rs397517902

Orientation

plus

Stabilized

plus

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

Make rs397517902(C;C)

Make rs397517902(C;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

156115274

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs397517902
dbSNP (classic)	rs397517902
ClinGen	rs397517902
ebi	rs397517902
HLI	rs397517902
Exac	rs397517902
Gnomad	rs397517902
Varsome	rs397517902
LitVar	rs397517902
Map	rs397517902
PheGenI	rs397517902
Biobank	rs397517902
1000 genomes	rs397517902
hgdp	rs397517902
ensembl	rs397517902
geneview	rs397517902
scholar	rs397517902
google	rs397517902
pharmgkb	rs397517902
gwascentral	rs397517902
openSNP	rs397517902
23andMe	rs397517902
SNPshot	rs397517902
SNPdbe	rs397517902
MSV3d	rs397517902
GWAS Ctlg	rs397517902

Max Magnitude

0

ClinVar
Risk	rs397517902(C;C)
Alt	rs397517902(C;C)
Reference	Rs397517902(G;G)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	LMNA
CLNDBN	not specified
Reversed	0
HGVS	NC_000001.10:g.156085065G>C
CLNSRC	ClinVar
CLNACC	RCV000041347.4,