rs587777492

Orientation

plus

Stabilized

minus

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

Make rs587777492(A;A)

Make rs587777492(A;G)

Reference

GRCh38 38.1/142

Chromosome

5

Position

45695795

Gene

HCN1

is a	snp
is	mentioned by
dbSNP	rs587777492
dbSNP (classic)	rs587777492
ClinGen	rs587777492
ebi	rs587777492
HLI	rs587777492
Exac	rs587777492
Gnomad	rs587777492
Varsome	rs587777492
LitVar	rs587777492
Map	rs587777492
PheGenI	rs587777492
Biobank	rs587777492
1000 genomes	rs587777492
hgdp	rs587777492
ensembl	rs587777492
geneview	rs587777492
scholar	rs587777492
google	rs587777492
pharmgkb	rs587777492
gwascentral	rs587777492
openSNP	rs587777492
23andMe	rs587777492
SNPshot	rs587777492
SNPdbe	rs587777492
MSV3d	rs587777492
GWAS Ctlg	rs587777492

Max Magnitude

0

ClinVar
Risk	rs587777492(A;A) Rs587777492(G;G)
Alt	rs587777492(A;A) Rs587777492(G;G)
Reference	Rs587777492(C;C)
Significance	Pathogenic
Disease	Epileptic encephalopathy
Variation	info
Gene	HCN1
CLNDBN	Epileptic encephalopathy, early infantile, 24
Reversed	1
HGVS	NC_000005.9:g.45695897G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000128459.3,