rs876657649

Orientation

plus

Stabilized

plus

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

Make rs876657649(C;G)

Make rs876657649(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

156136074

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs876657649
dbSNP (classic)	rs876657649
ClinGen	rs876657649
ebi	rs876657649
HLI	rs876657649
Exac	rs876657649
Gnomad	rs876657649
Varsome	rs876657649
LitVar	rs876657649
Map	rs876657649
PheGenI	rs876657649
Biobank	rs876657649
1000 genomes	rs876657649
hgdp	rs876657649
ensembl	rs876657649
geneview	rs876657649
scholar	rs876657649
google	rs876657649
pharmgkb	rs876657649
gwascentral	rs876657649
openSNP	rs876657649
23andMe	rs876657649
SNPshot	rs876657649
SNPdbe	rs876657649
MSV3d	rs876657649
GWAS Ctlg	rs876657649

Max Magnitude

0

ClinVar
Risk	rs876657649(G;G)
Alt	rs876657649(G;G)
Reference	Rs876657649(C;C)
Significance	Probable-Pathogenic
Disease	Laminopathy
Variation	info
Gene	LMNA
CLNDBN	Laminopathy
Reversed	0
HGVS	NC_000001.10:g.156105865C>G
CLNSRC
CLNACC	RCV000223064.1,