rs587777494

Orientation

plus

Stabilized

minus

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

Make rs587777494(C;G)

Reference

GRCh38 38.1/142

Chromosome

5

Position

45461967

Gene

HCN1

is a	snp
is	mentioned by
dbSNP	rs587777494
dbSNP (classic)	rs587777494
ClinGen	rs587777494
ebi	rs587777494
HLI	rs587777494
Exac	rs587777494
Gnomad	rs587777494
Varsome	rs587777494
LitVar	rs587777494
Map	rs587777494
PheGenI	rs587777494
Biobank	rs587777494
1000 genomes	rs587777494
hgdp	rs587777494
ensembl	rs587777494
geneview	rs587777494
scholar	rs587777494
google	rs587777494
pharmgkb	rs587777494
gwascentral	rs587777494
openSNP	rs587777494
23andMe	rs587777494
SNPshot	rs587777494
SNPdbe	rs587777494
MSV3d	rs587777494
GWAS Ctlg	rs587777494

Max Magnitude

0

ClinVar
Risk	Rs587777494(C;C)
Alt	Rs587777494(C;C)
Reference	Rs587777494(G;G)
Significance	Pathogenic
Disease	Epileptic encephalopathy
Variation	info
Gene	HCN1
CLNDBN	Epileptic encephalopathy, early infantile, 24
Reversed	1
HGVS	NC_000005.9:g.45462069C>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000128461.3,