rs786205418

Orientation

minus

Stabilized

minus

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

Make rs786205418(-;GTGA)

Make rs786205418(GTGA;GTGA)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

73343384

Gene	HCN4, LOC105370890

is a	snp
is	mentioned by
dbSNP	rs786205418
dbSNP (classic)	rs786205418
ClinGen	rs786205418
ebi	rs786205418
HLI	rs786205418
Exac	rs786205418
Gnomad	rs786205418
Varsome	rs786205418
LitVar	rs786205418
Map	rs786205418
PheGenI	rs786205418
Biobank	rs786205418
1000 genomes	rs786205418
hgdp	rs786205418
ensembl	rs786205418
geneview	rs786205418
scholar	rs786205418
google	rs786205418
pharmgkb	rs786205418
gwascentral	rs786205418
openSNP	rs786205418
23andMe	rs786205418
SNPshot	rs786205418
SNPdbe	rs786205418
MSV3d	rs786205418
GWAS Ctlg	rs786205418

Max Magnitude

0

ClinVar
Risk	rs786205418(GAGT;GAGT)
Alt	rs786205418(GAGT;GAGT)
Reference	Rs786205418(-;-)
Significance	Pathogenic
Disease	Brugada syndrome 8 Ventricular tachycardia
Variation	info
Gene	HCN4
CLNDBN	Brugada syndrome 8 Ventricular tachycardia
Reversed	1
HGVS	NC_000015.9:g.73635725_73635726insTCAC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000005485.4, RCV000171564.1,