rs587783533

Orientation

minus

Stabilized

minus

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

Make rs587783533(C;T)

Make rs587783533(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

111410181

Gene

DCX

is a	snp
is	mentioned by
dbSNP	rs587783533
dbSNP (classic)	rs587783533
ClinGen	rs587783533
ebi	rs587783533
HLI	rs587783533
Exac	rs587783533
Gnomad	rs587783533
Varsome	rs587783533
LitVar	rs587783533
Map	rs587783533
PheGenI	rs587783533
Biobank	rs587783533
1000 genomes	rs587783533
hgdp	rs587783533
ensembl	rs587783533
geneview	rs587783533
scholar	rs587783533
google	rs587783533
pharmgkb	rs587783533
gwascentral	rs587783533
openSNP	rs587783533
23andMe	rs587783533
SNPshot	rs587783533
SNPdbe	rs587783533
MSV3d	rs587783533
GWAS Ctlg	rs587783533

Max Magnitude

0

ClinVar
Risk	rs587783533(T;T)
Alt	rs587783533(T;T)
Reference	Rs587783533(C;C)
Significance	Pathogenic
Disease	Heterotopia
Variation	info
Gene	DCX
CLNDBN	Heterotopia
Reversed	1
HGVS	NC_000023.10:g.110653409G>A
CLNSRC
CLNACC	RCV000145821.1,