rs267607552

Orientation

plus

Stabilized

plus

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

Make rs267607552(A;A)

Make rs267607552(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

156136437

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs267607552
dbSNP (classic)	rs267607552
ClinGen	rs267607552
ebi	rs267607552
HLI	rs267607552
Exac	rs267607552
Gnomad	rs267607552
Varsome	rs267607552
LitVar	rs267607552
Map	rs267607552
PheGenI	rs267607552
Biobank	rs267607552
1000 genomes	rs267607552
hgdp	rs267607552
ensembl	rs267607552
geneview	rs267607552
scholar	rs267607552
google	rs267607552
pharmgkb	rs267607552
gwascentral	rs267607552
openSNP	rs267607552
23andMe	rs267607552
SNPshot	rs267607552
SNPdbe	rs267607552
MSV3d	rs267607552
GWAS Ctlg	rs267607552

Max Magnitude

0

ClinVar
Risk	rs267607552(A;A)
Alt	rs267607552(A;A)
Reference	Rs267607552(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	LMNA
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.156106228G>A
CLNSRC
CLNACC	RCV000057283.3,