rs587783564

Orientation

minus

Stabilized

minus

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

Make rs587783564(C;T)

Make rs587783564(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

111410344

Gene

DCX

is a	snp
is	mentioned by
dbSNP	rs587783564
dbSNP (classic)	rs587783564
ClinGen	rs587783564
ebi	rs587783564
HLI	rs587783564
Exac	rs587783564
Gnomad	rs587783564
Varsome	rs587783564
LitVar	rs587783564
Map	rs587783564
PheGenI	rs587783564
Biobank	rs587783564
1000 genomes	rs587783564
hgdp	rs587783564
ensembl	rs587783564
geneview	rs587783564
scholar	rs587783564
google	rs587783564
pharmgkb	rs587783564
gwascentral	rs587783564
openSNP	rs587783564
23andMe	rs587783564
SNPshot	rs587783564
SNPdbe	rs587783564
MSV3d	rs587783564
GWAS Ctlg	rs587783564

Max Magnitude

0

ClinVar
Risk	rs587783564(T;T)
Alt	rs587783564(T;T)
Reference	Rs587783564(C;C)
Significance	Pathogenic
Disease	Heterotopia
Variation	info
Gene	DCX
CLNDBN	Heterotopia
Reversed	1
HGVS	NC_000023.10:g.110653572G>A
CLNSRC
CLNACC	RCV000145861.1,