rs267607548

Orientation

plus

Stabilized

plus

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

Make rs267607548(A;A)

Make rs267607548(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

156136003

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs267607548
dbSNP (classic)	rs267607548
ClinGen	rs267607548
ebi	rs267607548
HLI	rs267607548
Exac	rs267607548
Gnomad	rs267607548
Varsome	rs267607548
LitVar	rs267607548
Map	rs267607548
PheGenI	rs267607548
Biobank	rs267607548
1000 genomes	rs267607548
hgdp	rs267607548
ensembl	rs267607548
geneview	rs267607548
scholar	rs267607548
google	rs267607548
pharmgkb	rs267607548
gwascentral	rs267607548
openSNP	rs267607548
23andMe	rs267607548
SNPshot	rs267607548
SNPdbe	rs267607548
MSV3d	rs267607548
GWAS Ctlg	rs267607548

Max Magnitude

0

ClinVar
Risk	rs267607548(A;A)
Alt	rs267607548(A;A)
Reference	Rs267607548(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	LMNA
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.156105794G>A
CLNSRC
CLNACC	RCV000057216.3,