rs267607582

Orientation

plus

Stabilized

plus

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

Make rs267607582(G;G)

Make rs267607582(G;T)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

156137642

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs267607582
dbSNP (classic)	rs267607582
ClinGen	rs267607582
ebi	rs267607582
HLI	rs267607582
Exac	rs267607582
Gnomad	rs267607582
Varsome	rs267607582
LitVar	rs267607582
Map	rs267607582
PheGenI	rs267607582
Biobank	rs267607582
1000 genomes	rs267607582
hgdp	rs267607582
ensembl	rs267607582
geneview	rs267607582
scholar	rs267607582
google	rs267607582
pharmgkb	rs267607582
gwascentral	rs267607582
openSNP	rs267607582
23andMe	rs267607582
SNPshot	rs267607582
SNPdbe	rs267607582
MSV3d	rs267607582
GWAS Ctlg	rs267607582

Max Magnitude

0

ClinVar
Risk	rs267607582(G;G)
Alt	rs267607582(G;G)
Reference	Rs267607582(T;T)
Significance	Pathogenic
Disease	Heart-hand syndrome not provided
Variation	info
Gene	LMNA
CLNDBN	Heart-hand syndrome, Slovenian type not provided
Reversed	0
HGVS	NC_000001.10:g.156107433T>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000015618.26, RCV000057337.1,