rs121908411

Orientation

minus

Stabilized

minus

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

Make rs121908411(C;C)

Make rs121908411(C;G)

Reference

GRCh38 38.1/141

Chromosome

15

Position

73329725

Gene

HCN4

is a	snp
is	mentioned by
dbSNP	rs121908411
dbSNP (classic)	rs121908411
ClinGen	rs121908411
ebi	rs121908411
HLI	rs121908411
Exac	rs121908411
Gnomad	rs121908411
Varsome	rs121908411
LitVar	rs121908411
Map	rs121908411
PheGenI	rs121908411
Biobank	rs121908411
1000 genomes	rs121908411
hgdp	rs121908411
ensembl	rs121908411
geneview	rs121908411
scholar	rs121908411
google	rs121908411
pharmgkb	rs121908411
gwascentral	rs121908411
openSNP	rs121908411
23andMe	rs121908411
SNPshot	rs121908411
SNPdbe	rs121908411
MSV3d	rs121908411
GWAS Ctlg	rs121908411

Max Magnitude

0

OMIM	605206
Desc
Variant	0004
Related	also

ClinVar
Risk	rs121908411(C;C)
Alt	rs121908411(C;C)
Reference	Rs121908411(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.73622066C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000005484.3,