rs587783579

Orientation

minus

Stabilized

minus

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

Make rs587783579(-;-)

Make rs587783579(-;A)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

111401014

Gene

DCX

is a	snp
is	mentioned by
dbSNP	rs587783579
dbSNP (classic)	rs587783579
ClinGen	rs587783579
ebi	rs587783579
HLI	rs587783579
Exac	rs587783579
Gnomad	rs587783579
Varsome	rs587783579
LitVar	rs587783579
Map	rs587783579
PheGenI	rs587783579
Biobank	rs587783579
1000 genomes	rs587783579
hgdp	rs587783579
ensembl	rs587783579
geneview	rs587783579
scholar	rs587783579
google	rs587783579
pharmgkb	rs587783579
gwascentral	rs587783579
openSNP	rs587783579
23andMe	rs587783579
SNPshot	rs587783579
SNPdbe	rs587783579
MSV3d	rs587783579
GWAS Ctlg	rs587783579

Max Magnitude

0

ClinVar
Risk	rs587783579(-;-)
Alt	rs587783579(-;-)
Reference	Rs587783579(A;A)
Significance	Pathogenic
Disease	Heterotopia
Variation	info
Gene	DCX
CLNDBN	Heterotopia
Reversed	1
HGVS	NC_000023.10:g.110644242delT
CLNSRC
CLNACC	RCV000145882.1,