rs587783534

Orientation

minus

Stabilized

minus

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

Make rs587783534(C;T)

Make rs587783534(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

111410173

Gene

DCX

is a	snp
is	mentioned by
dbSNP	rs587783534
dbSNP (classic)	rs587783534
ClinGen	rs587783534
ebi	rs587783534
HLI	rs587783534
Exac	rs587783534
Gnomad	rs587783534
Varsome	rs587783534
LitVar	rs587783534
Map	rs587783534
PheGenI	rs587783534
Biobank	rs587783534
1000 genomes	rs587783534
hgdp	rs587783534
ensembl	rs587783534
geneview	rs587783534
scholar	rs587783534
google	rs587783534
pharmgkb	rs587783534
gwascentral	rs587783534
openSNP	rs587783534
23andMe	rs587783534
SNPshot	rs587783534
SNPdbe	rs587783534
MSV3d	rs587783534
GWAS Ctlg	rs587783534

Max Magnitude

0

ClinVar
Risk	rs587783534(T;T)
Alt	rs587783534(T;T)
Reference	Rs587783534(C;C)
Significance	Probable-Pathogenic
Disease	Heterotopia
Variation	info
Gene	DCX
CLNDBN	Heterotopia
Reversed	1
HGVS	NC_000023.10:g.110653401G>A
CLNSRC
CLNACC	RCV000145822.1,