rs587783542

Orientation

minus

Stabilized

minus

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

Make rs587783542(A;T)

Make rs587783542(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

111410062

Gene

DCX

is a	snp
is	mentioned by
dbSNP	rs587783542
dbSNP (classic)	rs587783542
ClinGen	rs587783542
ebi	rs587783542
HLI	rs587783542
Exac	rs587783542
Gnomad	rs587783542
Varsome	rs587783542
LitVar	rs587783542
Map	rs587783542
PheGenI	rs587783542
Biobank	rs587783542
1000 genomes	rs587783542
hgdp	rs587783542
ensembl	rs587783542
geneview	rs587783542
scholar	rs587783542
google	rs587783542
pharmgkb	rs587783542
gwascentral	rs587783542
openSNP	rs587783542
23andMe	rs587783542
SNPshot	rs587783542
SNPdbe	rs587783542
MSV3d	rs587783542
GWAS Ctlg	rs587783542

Max Magnitude

0

ClinVar
Risk	rs587783542(T;T)
Alt	rs587783542(T;T)
Reference	Rs587783542(A;A)
Significance	Probable-Pathogenic
Disease	Heterotopia
Variation	info
Gene	DCX
CLNDBN	Heterotopia
Reversed	1
HGVS	NC_000023.10:g.110653290T>A
CLNSRC
CLNACC	RCV000145836.1,