rs794727637

Orientation

minus

Stabilized

minus

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

Make rs794727637(A;A)

Make rs794727637(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

73329719

Gene

HCN4

is a	snp
is	mentioned by
dbSNP	rs794727637
dbSNP (classic)	rs794727637
ClinGen	rs794727637
ebi	rs794727637
HLI	rs794727637
Exac	rs794727637
Gnomad	rs794727637
Varsome	rs794727637
LitVar	rs794727637
Map	rs794727637
PheGenI	rs794727637
Biobank	rs794727637
1000 genomes	rs794727637
hgdp	rs794727637
ensembl	rs794727637
geneview	rs794727637
scholar	rs794727637
google	rs794727637
pharmgkb	rs794727637
gwascentral	rs794727637
openSNP	rs794727637
23andMe	rs794727637
SNPshot	rs794727637
SNPdbe	rs794727637
MSV3d	rs794727637
GWAS Ctlg	rs794727637

Max Magnitude

0

ClinVar
Risk	rs794727637(A;A) rs794727637(C;C)
Alt	rs794727637(A;A) rs794727637(C;C)
Reference	Rs794727637(G;G)
Significance	Pathogenic
Disease	Sick sinus syndrome 2
Variation	info
Gene	HCN4
CLNDBN	Sick sinus syndrome 2, autosomal dominant
Reversed	1
HGVS	NC_000015.9:g.73622060C>G; NC_000015.9:g.73622060C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000415605.1, RCV000178241.2,