rs267607629

Orientation

plus

Stabilized

plus

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

Make rs267607629(C;G)

Make rs267607629(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

156134507

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs267607629
dbSNP (classic)	rs267607629
ClinGen	rs267607629
ebi	rs267607629
HLI	rs267607629
Exac	rs267607629
Gnomad	rs267607629
Varsome	rs267607629
LitVar	rs267607629
Map	rs267607629
PheGenI	rs267607629
Biobank	rs267607629
1000 genomes	rs267607629
hgdp	rs267607629
ensembl	rs267607629
geneview	rs267607629
scholar	rs267607629
google	rs267607629
pharmgkb	rs267607629
gwascentral	rs267607629
openSNP	rs267607629
23andMe	rs267607629
SNPshot	rs267607629
SNPdbe	rs267607629
MSV3d	rs267607629
GWAS Ctlg	rs267607629

Max Magnitude

0

ClinVar
Risk	rs267607629(G;G)
Alt	rs267607629(G;G)
Reference	Rs267607629(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	LMNA
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.156104298C>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000057431.3,