rs1057519276

Orientation

minus

Stabilized

minus

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

Make rs1057519276(C;G)

Make rs1057519276(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

15

Position

73332261

Gene

HCN4

is a	snp
is	mentioned by
dbSNP	rs1057519276
dbSNP (classic)	rs1057519276
ClinGen	rs1057519276
ebi	rs1057519276
HLI	rs1057519276
Exac	rs1057519276
Gnomad	rs1057519276
Varsome	rs1057519276
LitVar	rs1057519276
Map	rs1057519276
PheGenI	rs1057519276
Biobank	rs1057519276
1000 genomes	rs1057519276
hgdp	rs1057519276
ensembl	rs1057519276
geneview	rs1057519276
scholar	rs1057519276
google	rs1057519276
pharmgkb	rs1057519276
gwascentral	rs1057519276
openSNP	rs1057519276
23andMe	rs1057519276
SNPshot	rs1057519276
SNPdbe	rs1057519276
MSV3d	rs1057519276
GWAS Ctlg	rs1057519276

Max Magnitude

0

ClinVar
Risk	rs1057519276(G;G)
Alt	rs1057519276(G;G)
Reference	Rs1057519276(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.73624602G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000415571.1,