rs587783578

Orientation

minus

Stabilized

minus

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

Make rs587783578(-;-)

Make rs587783578(-;G)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

111401025

Gene

DCX

is a	snp
is	mentioned by
dbSNP	rs587783578
dbSNP (classic)	rs587783578
ClinGen	rs587783578
ebi	rs587783578
HLI	rs587783578
Exac	rs587783578
Gnomad	rs587783578
Varsome	rs587783578
LitVar	rs587783578
Map	rs587783578
PheGenI	rs587783578
Biobank	rs587783578
1000 genomes	rs587783578
hgdp	rs587783578
ensembl	rs587783578
geneview	rs587783578
scholar	rs587783578
google	rs587783578
pharmgkb	rs587783578
gwascentral	rs587783578
openSNP	rs587783578
23andMe	rs587783578
SNPshot	rs587783578
SNPdbe	rs587783578
MSV3d	rs587783578
GWAS Ctlg	rs587783578

Max Magnitude

0

ClinVar
Risk	rs587783578(-;-)
Alt	rs587783578(-;-)
Reference	Rs587783578(G;G)
Significance	Pathogenic
Disease	Heterotopia
Variation	info
Gene	DCX
CLNDBN	Heterotopia
Reversed	1
HGVS	NC_000023.10:g.110644253delC
CLNSRC
CLNACC	RCV000145881.1,