rs267607563

Orientation

plus

Stabilized

plus

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

Make rs267607563(A;A)

Make rs267607563(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

156136252

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs267607563
dbSNP (classic)	rs267607563
ClinGen	rs267607563
ebi	rs267607563
HLI	rs267607563
Exac	rs267607563
Gnomad	rs267607563
Varsome	rs267607563
LitVar	rs267607563
Map	rs267607563
PheGenI	rs267607563
Biobank	rs267607563
1000 genomes	rs267607563
hgdp	rs267607563
ensembl	rs267607563
geneview	rs267607563
scholar	rs267607563
google	rs267607563
pharmgkb	rs267607563
gwascentral	rs267607563
openSNP	rs267607563
23andMe	rs267607563
SNPshot	rs267607563
SNPdbe	rs267607563
MSV3d	rs267607563
GWAS Ctlg	rs267607563

Max Magnitude

0

ClinVar
Risk	rs267607563(A;A)
Alt	rs267607563(A;A)
Reference	Rs267607563(G;G)
Significance	Untested
Disease	not provided not specified
Variation	info
Gene	LMNA
CLNDBN	not provided not specified
Reversed	0
HGVS	NC_000001.10:g.156106043G>A
CLNSRC
CLNACC	RCV000057256.2, RCV000412674.1,