rs587783547

Orientation

minus

Stabilized

minus

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

Make rs587783547(A;A)

Make rs587783547(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

111401315

Gene

DCX

is a	snp
is	mentioned by
dbSNP	rs587783547
dbSNP (classic)	rs587783547
ClinGen	rs587783547
ebi	rs587783547
HLI	rs587783547
Exac	rs587783547
Gnomad	rs587783547
Varsome	rs587783547
LitVar	rs587783547
Map	rs587783547
PheGenI	rs587783547
Biobank	rs587783547
1000 genomes	rs587783547
hgdp	rs587783547
ensembl	rs587783547
geneview	rs587783547
scholar	rs587783547
google	rs587783547
pharmgkb	rs587783547
gwascentral	rs587783547
openSNP	rs587783547
23andMe	rs587783547
SNPshot	rs587783547
SNPdbe	rs587783547
MSV3d	rs587783547
GWAS Ctlg	rs587783547

Max Magnitude

0

ClinVar
Risk	rs587783547(A;A)
Alt	rs587783547(A;A)
Reference	Rs587783547(G;G)
Significance	Probable-Pathogenic
Disease	Heterotopia
Variation	info
Gene	DCX
CLNDBN	Heterotopia
Reversed	1
HGVS	NC_000023.10:g.110644543C>T
CLNSRC
CLNACC	RCV000145841.1,