rs587783573

Orientation

minus

Stabilized

minus

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

Make rs587783573(G;T)

Make rs587783573(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

111401067

Gene

DCX

is a	snp
is	mentioned by
dbSNP	rs587783573
dbSNP (classic)	rs587783573
ClinGen	rs587783573
ebi	rs587783573
HLI	rs587783573
Exac	rs587783573
Gnomad	rs587783573
Varsome	rs587783573
LitVar	rs587783573
Map	rs587783573
PheGenI	rs587783573
Biobank	rs587783573
1000 genomes	rs587783573
hgdp	rs587783573
ensembl	rs587783573
geneview	rs587783573
scholar	rs587783573
google	rs587783573
pharmgkb	rs587783573
gwascentral	rs587783573
openSNP	rs587783573
23andMe	rs587783573
SNPshot	rs587783573
SNPdbe	rs587783573
MSV3d	rs587783573
GWAS Ctlg	rs587783573

Max Magnitude

0

ClinVar
Risk	rs587783573(T;T)
Alt	rs587783573(T;T)
Reference	Rs587783573(G;G)
Significance	Pathogenic
Disease	Heterotopia
Variation	info
Gene	DCX
CLNDBN	Heterotopia
Reversed	1
HGVS	NC_000023.10:g.110644295C>A
CLNSRC
CLNACC	RCV000145876.1,