rs267607581

Orientation

plus

Stabilized

plus

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

Make rs267607581(C;G)

Make rs267607581(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

156137651

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs267607581
dbSNP (classic)	rs267607581
ClinGen	rs267607581
ebi	rs267607581
HLI	rs267607581
Exac	rs267607581
Gnomad	rs267607581
Varsome	rs267607581
LitVar	rs267607581
Map	rs267607581
PheGenI	rs267607581
Biobank	rs267607581
1000 genomes	rs267607581
hgdp	rs267607581
ensembl	rs267607581
geneview	rs267607581
scholar	rs267607581
google	rs267607581
pharmgkb	rs267607581
gwascentral	rs267607581
openSNP	rs267607581
23andMe	rs267607581
SNPshot	rs267607581
SNPdbe	rs267607581
MSV3d	rs267607581
GWAS Ctlg	rs267607581

Max Magnitude

0

ClinVar
Risk	rs267607581(G;G)
Alt	rs267607581(G;G)
Reference	Rs267607581(C;C)
Significance	Probable-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.156107442C>G
CLNSRC
CLNACC	RCV000057338.1, RCV000154514.1,