rs587783569

Orientation

minus

Stabilized

minus

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

Make rs587783569(C;C)

Make rs587783569(C;T)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

111401099

Gene

DCX

is a	snp
is	mentioned by
dbSNP	rs587783569
dbSNP (classic)	rs587783569
ClinGen	rs587783569
ebi	rs587783569
HLI	rs587783569
Exac	rs587783569
Gnomad	rs587783569
Varsome	rs587783569
LitVar	rs587783569
Map	rs587783569
PheGenI	rs587783569
Biobank	rs587783569
1000 genomes	rs587783569
hgdp	rs587783569
ensembl	rs587783569
geneview	rs587783569
scholar	rs587783569
google	rs587783569
pharmgkb	rs587783569
gwascentral	rs587783569
openSNP	rs587783569
23andMe	rs587783569
SNPshot	rs587783569
SNPdbe	rs587783569
MSV3d	rs587783569
GWAS Ctlg	rs587783569

Max Magnitude

0

ClinVar
Risk	rs587783569(C;C)
Alt	rs587783569(C;C)
Reference	Rs587783569(T;T)
Significance	Probable-Pathogenic
Disease	Heterotopia not provided
Variation	info
Gene	DCX
CLNDBN	Heterotopia not provided
Reversed	1
HGVS	NC_000023.10:g.110644327A>G
CLNSRC
CLNACC	RCV000145871.1, RCV000478870.1,