rs794728923

Merged into

rs397514251

Orientation

minus

Stabilized

minus

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

Make rs794728923(-;-)

Make rs794728923(-;CAGAAGCCC)

Reference

GRCh38.p2 38.2/146

Chromosome

3

Position

38555671

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs794728923
dbSNP (classic)	rs794728923
ClinGen	rs794728923
ebi	rs794728923
HLI	rs794728923
Exac	rs794728923
Gnomad	rs794728923
Varsome	rs794728923
LitVar	rs794728923
Map	rs794728923
PheGenI	rs794728923
Biobank	rs794728923
1000 genomes	rs794728923
hgdp	rs794728923
ensembl	rs794728923
geneview	rs794728923
scholar	rs794728923
google	rs794728923
pharmgkb	rs794728923
gwascentral	rs794728923
openSNP	rs794728923
23andMe	rs794728923
SNPshot	rs794728923
SNPdbe	rs794728923
MSV3d	rs794728923
GWAS Ctlg	rs794728923

Status

Merged into rs397514251

Max Magnitude

0

ClinVar
Risk
Alt
Reference	Rs794728923(CAGAAGCCC;CAGAAGCCC)
Significance	Pathogenic
Disease	Long QT syndrome 3 not provided
Variation	info
Gene	SCN5A
CLNDBN	Long QT syndrome 3 not provided
Reversed	1
HGVS	NC_000003.11:g.38597162_38597170delGGGCTTCTG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000009962.4, RCV000183165.2,