rs267607543

Orientation

plus

Stabilized

plus

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

Make rs267607543(C;C)

Make rs267607543(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

156137033

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs267607543
dbSNP (classic)	rs267607543
ClinGen	rs267607543
ebi	rs267607543
HLI	rs267607543
Exac	rs267607543
Gnomad	rs267607543
Varsome	rs267607543
LitVar	rs267607543
Map	rs267607543
PheGenI	rs267607543
Biobank	rs267607543
1000 genomes	rs267607543
hgdp	rs267607543
ensembl	rs267607543
geneview	rs267607543
scholar	rs267607543
google	rs267607543
pharmgkb	rs267607543
gwascentral	rs267607543
openSNP	rs267607543
23andMe	rs267607543
SNPshot	rs267607543
SNPdbe	rs267607543
MSV3d	rs267607543
GWAS Ctlg	rs267607543

Max Magnitude

0

ClinVar
Risk	rs267607543(A;A) rs267607543(C;C)
Alt	rs267607543(A;A) rs267607543(C;C)
Reference	Rs267607543(G;G)
Significance	Pathogenic
Disease	not provided Familial partial lipodystrophy 2
Variation	info
Gene	LMNA
CLNDBN	not provided Familial partial lipodystrophy 2
Reversed	0
HGVS	NC_000001.10:g.156106824G>A; NC_000001.10:g.156106824G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000057306.1, RCV000015610.27, RCV000057307.1,