rs886037666

Orientation

minus

Stabilized

minus

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

Make rs886037666(C;G)

Make rs886037666(G;G)

Reference

GRCh38.p7 38.3/149

Chromosome

1

Position

62634825

Gene

DOCK7

is a	snp
is	mentioned by
dbSNP	rs886037666
dbSNP (classic)	rs886037666
ClinGen	rs886037666
ebi	rs886037666
HLI	rs886037666
Exac	rs886037666
Gnomad	rs886037666
Varsome	rs886037666
LitVar	rs886037666
Map	rs886037666
PheGenI	rs886037666
Biobank	rs886037666
1000 genomes	rs886037666
hgdp	rs886037666
ensembl	rs886037666
geneview	rs886037666
scholar	rs886037666
google	rs886037666
pharmgkb	rs886037666
gwascentral	rs886037666
openSNP	rs886037666
23andMe	rs886037666
SNPshot	rs886037666
SNPdbe	rs886037666
MSV3d	rs886037666
GWAS Ctlg	rs886037666

Max Magnitude

0

ClinVar
Risk	rs886037666(G;G)
Alt	rs886037666(G;G)
Reference	Rs886037666(C;C)
Significance	Pathogenic
Disease	Epileptic encephalopathy
Variation	info
Gene	DOCK7
CLNDBN	Epileptic encephalopathy, early infantile, 23
Reversed	1
HGVS	NC_000001.10:g.63100496G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000128437.3,