rs1057519274

Orientation

minus

Stabilized

minus

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

Make rs1057519274(-;CAGCGTGCTCACC)

Make rs1057519274(CAGCGTGCTCACC;CAGCGTGCTCACC)

Reference

GRCh38.p7 38.3/150

Chromosome

15

Position

73325000

Gene

HCN4

is a	snp
is	mentioned by
dbSNP	rs1057519274
dbSNP (classic)	rs1057519274
ClinGen	rs1057519274
ebi	rs1057519274
HLI	rs1057519274
Exac	rs1057519274
Gnomad	rs1057519274
Varsome	rs1057519274
LitVar	rs1057519274
Map	rs1057519274
PheGenI	rs1057519274
Biobank	rs1057519274
1000 genomes	rs1057519274
hgdp	rs1057519274
ensembl	rs1057519274
geneview	rs1057519274
scholar	rs1057519274
google	rs1057519274
pharmgkb	rs1057519274
gwascentral	rs1057519274
openSNP	rs1057519274
23andMe	rs1057519274
SNPshot	rs1057519274
SNPdbe	rs1057519274
MSV3d	rs1057519274
GWAS Ctlg	rs1057519274

Max Magnitude

0

ClinVar
Risk	rs1057519274(CAGCGTGCTCACC;CAGCGTGCTCACC)
Alt	rs1057519274(CAGCGTGCTCACC;CAGCGTGCTCACC)
Reference	Rs1057519274(-;-)
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.73617342_73617354dupGGTGAGCACGCTG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000415565.1,