rs587783545

Orientation

minus

Stabilized

minus

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

Make rs587783545(-;-)

Make rs587783545(-;G)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

111401328

Gene

DCX

is a	snp
is	mentioned by
dbSNP	rs587783545
dbSNP (classic)	rs587783545
ClinGen	rs587783545
ebi	rs587783545
HLI	rs587783545
Exac	rs587783545
Gnomad	rs587783545
Varsome	rs587783545
LitVar	rs587783545
Map	rs587783545
PheGenI	rs587783545
Biobank	rs587783545
1000 genomes	rs587783545
hgdp	rs587783545
ensembl	rs587783545
geneview	rs587783545
scholar	rs587783545
google	rs587783545
pharmgkb	rs587783545
gwascentral	rs587783545
openSNP	rs587783545
23andMe	rs587783545
SNPshot	rs587783545
SNPdbe	rs587783545
MSV3d	rs587783545
GWAS Ctlg	rs587783545

Max Magnitude

0

ClinVar
Risk	rs587783545(-;-)
Alt	rs587783545(-;-)
Reference	Rs587783545(G;G)
Significance	Pathogenic
Disease	Heterotopia
Variation	info
Gene	DCX
CLNDBN	Heterotopia
Reversed	1
HGVS	NC_000023.10:g.110644556delC
CLNSRC
CLNACC	RCV000145839.1,