rs886037665

Orientation

minus

Stabilized

minus

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

Make rs886037665(-;-)

Make rs886037665(-;A)

Reference

GRCh38.p7 38.3/149

Chromosome

1

Position

62555911

Gene

DOCK7

is a	snp
is	mentioned by
dbSNP	rs886037665
dbSNP (classic)	rs886037665
ClinGen	rs886037665
ebi	rs886037665
HLI	rs886037665
Exac	rs886037665
Gnomad	rs886037665
Varsome	rs886037665
LitVar	rs886037665
Map	rs886037665
PheGenI	rs886037665
Biobank	rs886037665
1000 genomes	rs886037665
hgdp	rs886037665
ensembl	rs886037665
geneview	rs886037665
scholar	rs886037665
google	rs886037665
pharmgkb	rs886037665
gwascentral	rs886037665
openSNP	rs886037665
23andMe	rs886037665
SNPshot	rs886037665
SNPdbe	rs886037665
MSV3d	rs886037665
GWAS Ctlg	rs886037665

Max Magnitude

0

ClinVar
Risk	rs886037665(-;-)
Alt	rs886037665(-;-)
Reference	Rs886037665(A;A)
Significance	Pathogenic
Disease	Epileptic encephalopathy
Variation	info
Gene	DOCK7
CLNDBN	Epileptic encephalopathy, early infantile, 23
Reversed	1
HGVS	NC_000001.10:g.63021582delT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000128435.3,