rs794728605

Orientation

plus

Stabilized

plus

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

Make rs794728605(GAT;TGGTCACCTGAGAG)

Make rs794728605(TGGTCACCTGAGAG;TGGTCACCTGAGAG)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

156130641

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs794728605
dbSNP (classic)	rs794728605
ClinGen	rs794728605
ebi	rs794728605
HLI	rs794728605
Exac	rs794728605
Gnomad	rs794728605
Varsome	rs794728605
LitVar	rs794728605
Map	rs794728605
PheGenI	rs794728605
Biobank	rs794728605
1000 genomes	rs794728605
hgdp	rs794728605
ensembl	rs794728605
geneview	rs794728605
scholar	rs794728605
google	rs794728605
pharmgkb	rs794728605
gwascentral	rs794728605
openSNP	rs794728605
23andMe	rs794728605
SNPshot	rs794728605
SNPdbe	rs794728605
MSV3d	rs794728605
GWAS Ctlg	rs794728605

Max Magnitude

0

ClinVar
Risk	rs794728605(TGGTCACCTGAGAG;TGGTCACCTGAGAG)
Alt	rs794728605(TGGTCACCTGAGAG;TGGTCACCTGAGAG)
Reference	Rs794728605(GAT;GAT)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	LMNA
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.156100432_156100434delGATinsTGGTCACCTGAGAG
CLNSRC
CLNACC	RCV000182386.3,