rs104894485

Orientation

minus

Stabilized

minus

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

Make rs104894485(A;A)

Make rs104894485(A;G)

Reference

GRCh38 38.1/141

Chromosome

15

Position

73325378

Gene

HCN4

is a	snp
is	mentioned by
dbSNP	rs104894485
dbSNP (classic)	rs104894485
ClinGen	rs104894485
ebi	rs104894485
HLI	rs104894485
Exac	rs104894485
Gnomad	rs104894485
Varsome	rs104894485
LitVar	rs104894485
Map	rs104894485
PheGenI	rs104894485
Biobank	rs104894485
1000 genomes	rs104894485
hgdp	rs104894485
ensembl	rs104894485
geneview	rs104894485
scholar	rs104894485
google	rs104894485
pharmgkb	rs104894485
gwascentral	rs104894485
openSNP	rs104894485
23andMe	rs104894485
SNPshot	rs104894485
SNPdbe	rs104894485
MSV3d	rs104894485
GWAS Ctlg	rs104894485

Max Magnitude

0

OMIM	605206
Desc
Variant	0003
Related	also

ClinVar
Risk	rs104894485(A;A)
Alt	rs104894485(A;A)
Reference	Rs104894485(G;G)
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.73617719C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000005483.3,