rs587783554

Orientation

minus

Stabilized

minus

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

Make rs587783554(C;T)

Make rs587783554(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

111401217

Gene

DCX

is a	snp
is	mentioned by
dbSNP	rs587783554
dbSNP (classic)	rs587783554
ClinGen	rs587783554
ebi	rs587783554
HLI	rs587783554
Exac	rs587783554
Gnomad	rs587783554
Varsome	rs587783554
LitVar	rs587783554
Map	rs587783554
PheGenI	rs587783554
Biobank	rs587783554
1000 genomes	rs587783554
hgdp	rs587783554
ensembl	rs587783554
geneview	rs587783554
scholar	rs587783554
google	rs587783554
pharmgkb	rs587783554
gwascentral	rs587783554
openSNP	rs587783554
23andMe	rs587783554
SNPshot	rs587783554
SNPdbe	rs587783554
MSV3d	rs587783554
GWAS Ctlg	rs587783554

Max Magnitude

0

ClinVar
Risk	rs587783554(T;T)
Alt	rs587783554(T;T)
Reference	Rs587783554(C;C)
Significance	Pathogenic
Disease	Heterotopia
Variation	info
Gene	DCX
CLNDBN	Heterotopia
Reversed	1
HGVS	NC_000023.10:g.110644445G>A
CLNSRC
CLNACC	RCV000145849.1,