rs587783592

Orientation

minus

Stabilized

minus

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

Make rs587783592(C;T)

Make rs587783592(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

111330943

Gene

DCX

is a	snp
is	mentioned by
dbSNP	rs587783592
dbSNP (classic)	rs587783592
ClinGen	rs587783592
ebi	rs587783592
HLI	rs587783592
Exac	rs587783592
Gnomad	rs587783592
Varsome	rs587783592
LitVar	rs587783592
Map	rs587783592
PheGenI	rs587783592
Biobank	rs587783592
1000 genomes	rs587783592
hgdp	rs587783592
ensembl	rs587783592
geneview	rs587783592
scholar	rs587783592
google	rs587783592
pharmgkb	rs587783592
gwascentral	rs587783592
openSNP	rs587783592
23andMe	rs587783592
SNPshot	rs587783592
SNPdbe	rs587783592
MSV3d	rs587783592
GWAS Ctlg	rs587783592

Max Magnitude

0

ClinVar
Risk	rs587783592(T;T)
Alt	rs587783592(T;T)
Reference	Rs587783592(C;C)
Significance	Pathogenic
Disease	Heterotopia not provided
Variation	info
Gene	DCX
CLNDBN	Heterotopia not provided
Reversed	1
HGVS	NC_000023.10:g.110574171G>A
CLNSRC
CLNACC	RCV000145895.1, RCV000493373.1,