rs587783591

Orientation

minus

Stabilized

minus

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

Make rs587783591(A;T)

Make rs587783591(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

111330997

Gene

DCX

is a	snp
is	mentioned by
dbSNP	rs587783591
dbSNP (classic)	rs587783591
ClinGen	rs587783591
ebi	rs587783591
HLI	rs587783591
Exac	rs587783591
Gnomad	rs587783591
Varsome	rs587783591
LitVar	rs587783591
Map	rs587783591
PheGenI	rs587783591
Biobank	rs587783591
1000 genomes	rs587783591
hgdp	rs587783591
ensembl	rs587783591
geneview	rs587783591
scholar	rs587783591
google	rs587783591
pharmgkb	rs587783591
gwascentral	rs587783591
openSNP	rs587783591
23andMe	rs587783591
SNPshot	rs587783591
SNPdbe	rs587783591
MSV3d	rs587783591
GWAS Ctlg	rs587783591

Max Magnitude

0

ClinVar
Risk	rs587783591(T;T)
Alt	rs587783591(T;T)
Reference	Rs587783591(A;A)
Significance	Pathogenic
Disease	Heterotopia
Variation	info
Gene	DCX
CLNDBN	Heterotopia
Reversed	1
HGVS	NC_000023.10:g.110574225T>A
CLNSRC
CLNACC	RCV000145894.1,