rs587783565

Orientation

minus

Stabilized

minus

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

Make rs587783565(A;A)

Make rs587783565(A;C)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

111401124

Gene

DCX

is a	snp
is	mentioned by
dbSNP	rs587783565
dbSNP (classic)	rs587783565
ClinGen	rs587783565
ebi	rs587783565
HLI	rs587783565
Exac	rs587783565
Gnomad	rs587783565
Varsome	rs587783565
LitVar	rs587783565
Map	rs587783565
PheGenI	rs587783565
Biobank	rs587783565
1000 genomes	rs587783565
hgdp	rs587783565
ensembl	rs587783565
geneview	rs587783565
scholar	rs587783565
google	rs587783565
pharmgkb	rs587783565
gwascentral	rs587783565
openSNP	rs587783565
23andMe	rs587783565
SNPshot	rs587783565
SNPdbe	rs587783565
MSV3d	rs587783565
GWAS Ctlg	rs587783565

Max Magnitude

0

ClinVar
Risk	rs587783565(A;A)
Alt	rs587783565(A;A)
Reference	Rs587783565(C;C)
Significance	Probable-Pathogenic
Disease	Heterotopia
Variation	info
Gene	DCX
CLNDBN	Heterotopia
Reversed	1
HGVS	NC_000023.10:g.110644352G>T
CLNSRC
CLNACC	RCV000145862.1,