rs587783538

Orientation

minus

Stabilized

minus

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

Make rs587783538(A;A)

Make rs587783538(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

111410100

Gene

DCX

is a	snp
is	mentioned by
dbSNP	rs587783538
dbSNP (classic)	rs587783538
ClinGen	rs587783538
ebi	rs587783538
HLI	rs587783538
Exac	rs587783538
Gnomad	rs587783538
Varsome	rs587783538
LitVar	rs587783538
Map	rs587783538
PheGenI	rs587783538
Biobank	rs587783538
1000 genomes	rs587783538
hgdp	rs587783538
ensembl	rs587783538
geneview	rs587783538
scholar	rs587783538
google	rs587783538
pharmgkb	rs587783538
gwascentral	rs587783538
openSNP	rs587783538
23andMe	rs587783538
SNPshot	rs587783538
SNPdbe	rs587783538
MSV3d	rs587783538
GWAS Ctlg	rs587783538

Max Magnitude

0

ClinVar
Risk	rs587783538(A;A) rs587783538(T;T)
Alt	rs587783538(A;A) rs587783538(T;T)
Reference	Rs587783538(G;G)
Significance	Pathogenic
Disease	Heterotopia
Variation	info
Gene	DCX
CLNDBN	Heterotopia
Reversed	1
HGVS	NC_000023.10:g.110653328C>A; NC_000023.10:g.110653328C>T
CLNSRC
CLNACC	RCV000145830.1, RCV000145829.1,