rs587777485

Orientation

plus

Stabilized

minus

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

Make rs587777485(A;A)

Make rs587777485(A;C)

Reference

GRCh38 38.1/142

Chromosome

1

Position

62457653

Gene

DOCK7

is a	snp
is	mentioned by
dbSNP	rs587777485
dbSNP (classic)	rs587777485
ClinGen	rs587777485
ebi	rs587777485
HLI	rs587777485
Exac	rs587777485
Gnomad	rs587777485
Varsome	rs587777485
LitVar	rs587777485
Map	rs587777485
PheGenI	rs587777485
Biobank	rs587777485
1000 genomes	rs587777485
hgdp	rs587777485
ensembl	rs587777485
geneview	rs587777485
scholar	rs587777485
google	rs587777485
pharmgkb	rs587777485
gwascentral	rs587777485
openSNP	rs587777485
23andMe	rs587777485
SNPshot	rs587777485
SNPdbe	rs587777485
MSV3d	rs587777485
GWAS Ctlg	rs587777485

Max Magnitude

0

ClinVar
Risk	rs587777485(A;A) Rs587777485(C;C)
Alt	rs587777485(A;A) Rs587777485(C;C)
Reference	Rs587777485(G;G)
Significance	Pathogenic
Disease	Epileptic encephalopathy
Variation	info
Gene	DOCK7
CLNDBN	Epileptic encephalopathy, early infantile, 23
Reversed	1
HGVS	NC_000001.10:g.62923324C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000128438.3,