rs267607592

Orientation

plus

Stabilized

plus

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

Make rs267607592(A;A)

Make rs267607592(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

156137233

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs267607592
dbSNP (classic)	rs267607592
ClinGen	rs267607592
ebi	rs267607592
HLI	rs267607592
Exac	rs267607592
Gnomad	rs267607592
Varsome	rs267607592
LitVar	rs267607592
Map	rs267607592
PheGenI	rs267607592
Biobank	rs267607592
1000 genomes	rs267607592
hgdp	rs267607592
ensembl	rs267607592
geneview	rs267607592
scholar	rs267607592
google	rs267607592
pharmgkb	rs267607592
gwascentral	rs267607592
openSNP	rs267607592
23andMe	rs267607592
SNPshot	rs267607592
SNPdbe	rs267607592
MSV3d	rs267607592
GWAS Ctlg	rs267607592

Max Magnitude

0

ClinVar
Risk	rs267607592(A;A)
Alt	rs267607592(A;A)
Reference	Rs267607592(G;G)
Significance	Pathogenic
Disease	not provided Limb-girdle muscular dystrophy
Variation	info
Gene	LMNA
CLNDBN	not provided Limb-girdle muscular dystrophy
Reversed	0
HGVS	NC_000001.10:g.156107024G>A
CLNSRC
CLNACC	RCV000057335.1, RCV000150954.1,