rs1057519015

Orientation

minus

Stabilized

minus

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

Make rs1057519015(-;-)

Make rs1057519015(-;C)

Reference

GRCh38.p7 38.3/150

Chromosome

15

Position

73325404

Gene

HCN4

is a	snp
is	mentioned by
dbSNP	rs1057519015
dbSNP (classic)	rs1057519015
ClinGen	rs1057519015
ebi	rs1057519015
HLI	rs1057519015
Exac	rs1057519015
Gnomad	rs1057519015
Varsome	rs1057519015
LitVar	rs1057519015
Map	rs1057519015
PheGenI	rs1057519015
Biobank	rs1057519015
1000 genomes	rs1057519015
hgdp	rs1057519015
ensembl	rs1057519015
geneview	rs1057519015
scholar	rs1057519015
google	rs1057519015
pharmgkb	rs1057519015
gwascentral	rs1057519015
openSNP	rs1057519015
23andMe	rs1057519015
SNPshot	rs1057519015
SNPdbe	rs1057519015
MSV3d	rs1057519015
GWAS Ctlg	rs1057519015

Max Magnitude

0

ClinVar
Risk	rs1057519015(-;-)
Alt	rs1057519015(-;-)
Reference	Rs1057519015(C;C)
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.73617745delG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000005482.2,