rs587783566

Orientation

minus

Stabilized

minus

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

Make rs587783566(C;G)

Make rs587783566(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

111401123

Gene

DCX

is a	snp
is	mentioned by
dbSNP	rs587783566
dbSNP (classic)	rs587783566
ClinGen	rs587783566
ebi	rs587783566
HLI	rs587783566
Exac	rs587783566
Gnomad	rs587783566
Varsome	rs587783566
LitVar	rs587783566
Map	rs587783566
PheGenI	rs587783566
Biobank	rs587783566
1000 genomes	rs587783566
hgdp	rs587783566
ensembl	rs587783566
geneview	rs587783566
scholar	rs587783566
google	rs587783566
pharmgkb	rs587783566
gwascentral	rs587783566
openSNP	rs587783566
23andMe	rs587783566
SNPshot	rs587783566
SNPdbe	rs587783566
MSV3d	rs587783566
GWAS Ctlg	rs587783566

Max Magnitude

0

ClinVar
Risk	rs587783566(G;G)
Alt	rs587783566(G;G)
Reference	Rs587783566(C;C)
Significance	Pathogenic
Disease	Heterotopia
Variation	info
Gene	DCX
CLNDBN	Heterotopia
Reversed	1
HGVS	NC_000023.10:g.110644351G>C
CLNSRC
CLNACC	RCV000145863.1,