rs587783590

Orientation

minus

Stabilized

minus

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

Make rs587783590(C;T)

Make rs587783590(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

111331036

Gene

DCX

is a	snp
is	mentioned by
dbSNP	rs587783590
dbSNP (classic)	rs587783590
ClinGen	rs587783590
ebi	rs587783590
HLI	rs587783590
Exac	rs587783590
Gnomad	rs587783590
Varsome	rs587783590
LitVar	rs587783590
Map	rs587783590
PheGenI	rs587783590
Biobank	rs587783590
1000 genomes	rs587783590
hgdp	rs587783590
ensembl	rs587783590
geneview	rs587783590
scholar	rs587783590
google	rs587783590
pharmgkb	rs587783590
gwascentral	rs587783590
openSNP	rs587783590
23andMe	rs587783590
SNPshot	rs587783590
SNPdbe	rs587783590
MSV3d	rs587783590
GWAS Ctlg	rs587783590

Max Magnitude

0

ClinVar
Risk	rs587783590(T;T)
Alt	rs587783590(T;T)
Reference	Rs587783590(C;C)
Significance	Pathogenic
Disease	Heterotopia not provided
Variation	info
Gene	DCX
CLNDBN	Heterotopia not provided
Reversed	1
HGVS	NC_000023.10:g.110574264G>A
CLNSRC
CLNACC	RCV000145893.1, RCV000255524.1,