rs1057519275

Orientation

minus

Stabilized

minus

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

Make rs1057519275(C;C)

Make rs1057519275(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

15

Position

73329722

Gene

HCN4

is a	snp
is	mentioned by
dbSNP	rs1057519275
dbSNP (classic)	rs1057519275
ClinGen	rs1057519275
ebi	rs1057519275
HLI	rs1057519275
Exac	rs1057519275
Gnomad	rs1057519275
Varsome	rs1057519275
LitVar	rs1057519275
Map	rs1057519275
PheGenI	rs1057519275
Biobank	rs1057519275
1000 genomes	rs1057519275
hgdp	rs1057519275
ensembl	rs1057519275
geneview	rs1057519275
scholar	rs1057519275
google	rs1057519275
pharmgkb	rs1057519275
gwascentral	rs1057519275
openSNP	rs1057519275
23andMe	rs1057519275
SNPshot	rs1057519275
SNPdbe	rs1057519275
MSV3d	rs1057519275
GWAS Ctlg	rs1057519275

Max Magnitude

0

ClinVar
Risk	rs1057519275(C;C)
Alt	rs1057519275(C;C)
Reference	Rs1057519275(T;T)
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.73622063A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000415538.1,