rs876661352

Orientation

plus

Stabilized

plus

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

Make rs876661352(-;-)

Make rs876661352(-;CT)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

156135931

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs876661352
dbSNP (classic)	rs876661352
ClinGen	rs876661352
ebi	rs876661352
HLI	rs876661352
Exac	rs876661352
Gnomad	rs876661352
Varsome	rs876661352
LitVar	rs876661352
Map	rs876661352
PheGenI	rs876661352
Biobank	rs876661352
1000 genomes	rs876661352
hgdp	rs876661352
ensembl	rs876661352
geneview	rs876661352
scholar	rs876661352
google	rs876661352
pharmgkb	rs876661352
gwascentral	rs876661352
openSNP	rs876661352
23andMe	rs876661352
SNPshot	rs876661352
SNPdbe	rs876661352
MSV3d	rs876661352
GWAS Ctlg	rs876661352

Max Magnitude

0

ClinVar
Risk	rs876661352(-;-)
Alt	rs876661352(-;-)
Reference	Rs876661352(CT;CT)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	LMNA
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.156105722_156105723delCT
CLNSRC
CLNACC	RCV000223918.1,