rs587783582

Orientation

minus

Stabilized

minus

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

Make rs587783582(A;A)

Make rs587783582(A;T)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

111333135

Gene

DCX

is a	snp
is	mentioned by
dbSNP	rs587783582
dbSNP (classic)	rs587783582
ClinGen	rs587783582
ebi	rs587783582
HLI	rs587783582
Exac	rs587783582
Gnomad	rs587783582
Varsome	rs587783582
LitVar	rs587783582
Map	rs587783582
PheGenI	rs587783582
Biobank	rs587783582
1000 genomes	rs587783582
hgdp	rs587783582
ensembl	rs587783582
geneview	rs587783582
scholar	rs587783582
google	rs587783582
pharmgkb	rs587783582
gwascentral	rs587783582
openSNP	rs587783582
23andMe	rs587783582
SNPshot	rs587783582
SNPdbe	rs587783582
MSV3d	rs587783582
GWAS Ctlg	rs587783582

Max Magnitude

0

ClinVar
Risk	rs587783582(A;A)
Alt	rs587783582(A;A)
Reference	Rs587783582(T;T)
Significance	Probable-Pathogenic
Disease	Heterotopia
Variation	info
Gene	DCX
CLNDBN	Heterotopia
Reversed	1
HGVS	NC_000023.10:g.110576363A>T
CLNSRC
CLNACC	RCV000145885.1,