rs267607572

Orientation

plus

Stabilized

plus

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

Make rs267607572(G;G)

Make rs267607572(G;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

156134518

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs267607572
dbSNP (classic)	rs267607572
ClinGen	rs267607572
ebi	rs267607572
HLI	rs267607572
Exac	rs267607572
Gnomad	rs267607572
Varsome	rs267607572
LitVar	rs267607572
Map	rs267607572
PheGenI	rs267607572
Biobank	rs267607572
1000 genomes	rs267607572
hgdp	rs267607572
ensembl	rs267607572
geneview	rs267607572
scholar	rs267607572
google	rs267607572
pharmgkb	rs267607572
gwascentral	rs267607572
openSNP	rs267607572
23andMe	rs267607572
SNPshot	rs267607572
SNPdbe	rs267607572
MSV3d	rs267607572
GWAS Ctlg	rs267607572

Max Magnitude

0

ClinVar
Risk	rs267607572(G;G)
Alt	rs267607572(G;G)
Reference	Rs267607572(T;T)
Significance	Untested
Disease	not specified not provided
Variation	info
Gene	LMNA
CLNDBN	not specified not provided
Reversed	0
HGVS	NC_000001.10:g.156104309T>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000041357.2, RCV000057435.1,