rs104894488

Orientation

minus

Stabilized

minus

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

Make rs104894488(A;A)

Make rs104894488(A;C)

Reference

GRCh38 38.1/141

Chromosome

15

Position

73324216

Gene

HCN4

is a	snp
is	mentioned by
dbSNP	rs104894488
dbSNP (classic)	rs104894488
ClinGen	rs104894488
ebi	rs104894488
HLI	rs104894488
Exac	rs104894488
Gnomad	rs104894488
Varsome	rs104894488
LitVar	rs104894488
Map	rs104894488
PheGenI	rs104894488
Biobank	rs104894488
1000 genomes	rs104894488
hgdp	rs104894488
ensembl	rs104894488
geneview	rs104894488
scholar	rs104894488
google	rs104894488
pharmgkb	rs104894488
gwascentral	rs104894488
openSNP	rs104894488
23andMe	rs104894488
SNPshot	rs104894488
SNPdbe	rs104894488
MSV3d	rs104894488
GWAS Ctlg	rs104894488

Max Magnitude

0

OMIM	605206
Desc
Variant	0001
Related	also

ClinVar
Risk	rs104894488(A;A) rs104894488(T;T)
Alt	rs104894488(A;A) rs104894488(T;T)
Reference	Rs104894488(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.73616557G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000005481.3,