rs786205259

Orientation

minus

Stabilized

minus

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

Make rs786205259(-;-)

Make rs786205259(-;TTTG)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

73322592

Gene

HCN4

is a	snp
is	mentioned by
dbSNP	rs786205259
dbSNP (classic)	rs786205259
ClinGen	rs786205259
ebi	rs786205259
HLI	rs786205259
Exac	rs786205259
Gnomad	rs786205259
Varsome	rs786205259
LitVar	rs786205259
Map	rs786205259
PheGenI	rs786205259
Biobank	rs786205259
1000 genomes	rs786205259
hgdp	rs786205259
ensembl	rs786205259
geneview	rs786205259
scholar	rs786205259
google	rs786205259
pharmgkb	rs786205259
gwascentral	rs786205259
openSNP	rs786205259
23andMe	rs786205259
SNPshot	rs786205259
SNPdbe	rs786205259
MSV3d	rs786205259
GWAS Ctlg	rs786205259

Max Magnitude

0

ClinVar
Risk	rs786205259(-;-)
Alt	rs786205259(-;-)
Reference	Rs786205259(TTTG;TTTG)
Significance	Probable-Pathogenic
Disease	Sinus node disease
Variation	info
Gene	HCN4
CLNDBN	Sinus node disease
Reversed	1
HGVS	NC_000015.9:g.73614933_73614936delCAAA
CLNSRC
CLNACC	RCV000171563.1,