rs587783532

Orientation

minus

Stabilized

minus

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

Make rs587783532(A;A)

Make rs587783532(A;C)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

111410189

Gene

DCX

is a	snp
is	mentioned by
dbSNP	rs587783532
dbSNP (classic)	rs587783532
ClinGen	rs587783532
ebi	rs587783532
HLI	rs587783532
Exac	rs587783532
Gnomad	rs587783532
Varsome	rs587783532
LitVar	rs587783532
Map	rs587783532
PheGenI	rs587783532
Biobank	rs587783532
1000 genomes	rs587783532
hgdp	rs587783532
ensembl	rs587783532
geneview	rs587783532
scholar	rs587783532
google	rs587783532
pharmgkb	rs587783532
gwascentral	rs587783532
openSNP	rs587783532
23andMe	rs587783532
SNPshot	rs587783532
SNPdbe	rs587783532
MSV3d	rs587783532
GWAS Ctlg	rs587783532

Max Magnitude

0

ClinVar
Risk	rs587783532(A;A)
Alt	rs587783532(A;A)
Reference	Rs587783532(C;C)
Significance	Pathogenic
Disease	Heterotopia
Variation	info
Gene	DCX
CLNDBN	Heterotopia
Reversed	1
HGVS	NC_000023.10:g.110653417G>T
CLNSRC
CLNACC	RCV000145820.1,