rs267607570

Orientation

plus

Stabilized

plus

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

Make rs267607570(C;C)

Make rs267607570(C;G)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

156130757

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs267607570
dbSNP (classic)	rs267607570
ClinGen	rs267607570
ebi	rs267607570
HLI	rs267607570
Exac	rs267607570
Gnomad	rs267607570
Varsome	rs267607570
LitVar	rs267607570
Map	rs267607570
PheGenI	rs267607570
Biobank	rs267607570
1000 genomes	rs267607570
hgdp	rs267607570
ensembl	rs267607570
geneview	rs267607570
scholar	rs267607570
google	rs267607570
pharmgkb	rs267607570
gwascentral	rs267607570
openSNP	rs267607570
23andMe	rs267607570
SNPshot	rs267607570
SNPdbe	rs267607570
MSV3d	rs267607570
GWAS Ctlg	rs267607570

Max Magnitude

0

ClinVar
Risk	rs267607570(A;A) rs267607570(C;C)
Alt	rs267607570(A;A) rs267607570(C;C)
Reference	Rs267607570(G;G)
Significance	Pathogenic
Disease	not specified not provided
Variation	info
Gene	LMNA
CLNDBN	not specified not provided
Reversed	0
HGVS	NC_000001.10:g.156100548G>A; NC_000001.10:g.156100548G>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000150939.1, RCV000057411.4,