rs267607571

Orientation

plus

Stabilized

plus

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

Make rs267607571(A;A)

Make rs267607571(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

156134458

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs267607571
dbSNP (classic)	rs267607571
ClinGen	rs267607571
ebi	rs267607571
HLI	rs267607571
Exac	rs267607571
Gnomad	rs267607571
Varsome	rs267607571
LitVar	rs267607571
Map	rs267607571
PheGenI	rs267607571
Biobank	rs267607571
1000 genomes	rs267607571
hgdp	rs267607571
ensembl	rs267607571
geneview	rs267607571
scholar	rs267607571
google	rs267607571
pharmgkb	rs267607571
gwascentral	rs267607571
openSNP	rs267607571
23andMe	rs267607571
SNPshot	rs267607571
SNPdbe	rs267607571
MSV3d	rs267607571
GWAS Ctlg	rs267607571

Max Magnitude

0

ClinVar
Risk	rs267607571(A;A)
Alt	rs267607571(A;A)
Reference	Rs267607571(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	LMNA
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.156104249G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000057421.3,