rs587777495

Orientation

plus

Stabilized

minus

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

Make rs587777495(A;A)

Make rs587777495(A;G)

Reference

GRCh38 38.1/142

Chromosome

5

Position

45645199

Gene

HCN1

is a	snp
is	mentioned by
dbSNP	rs587777495
dbSNP (classic)	rs587777495
ClinGen	rs587777495
ebi	rs587777495
HLI	rs587777495
Exac	rs587777495
Gnomad	rs587777495
Varsome	rs587777495
LitVar	rs587777495
Map	rs587777495
PheGenI	rs587777495
Biobank	rs587777495
1000 genomes	rs587777495
hgdp	rs587777495
ensembl	rs587777495
geneview	rs587777495
scholar	rs587777495
google	rs587777495
pharmgkb	rs587777495
gwascentral	rs587777495
openSNP	rs587777495
23andMe	rs587777495
SNPshot	rs587777495
SNPdbe	rs587777495
MSV3d	rs587777495
GWAS Ctlg	rs587777495

Max Magnitude

0

ClinVar
Risk	rs587777495(A;A) Rs587777495(G;G)
Alt	rs587777495(A;A) Rs587777495(G;G)
Reference	Rs587777495(C;C)
Significance	Pathogenic
Disease	Epileptic encephalopathy
Variation	info
Gene	HCN1
CLNDBN	Epileptic encephalopathy, early infantile, 24
Reversed	1
HGVS	NC_000005.9:g.45645301G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000128462.3,