rs587783586

Orientation

minus

Stabilized

minus

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

Make rs587783586(A;T)

Make rs587783586(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

111333093

Gene

DCX

is a	snp
is	mentioned by
dbSNP	rs587783586
dbSNP (classic)	rs587783586
ClinGen	rs587783586
ebi	rs587783586
HLI	rs587783586
Exac	rs587783586
Gnomad	rs587783586
Varsome	rs587783586
LitVar	rs587783586
Map	rs587783586
PheGenI	rs587783586
Biobank	rs587783586
1000 genomes	rs587783586
hgdp	rs587783586
ensembl	rs587783586
geneview	rs587783586
scholar	rs587783586
google	rs587783586
pharmgkb	rs587783586
gwascentral	rs587783586
openSNP	rs587783586
23andMe	rs587783586
SNPshot	rs587783586
SNPdbe	rs587783586
MSV3d	rs587783586
GWAS Ctlg	rs587783586

Max Magnitude

0

ClinVar
Risk	rs587783586(T;T)
Alt	rs587783586(T;T)
Reference	Rs587783586(A;A)
Significance	Pathogenic
Disease	Heterotopia
Variation	info
Gene	DCX
CLNDBN	Heterotopia
Reversed	1
HGVS	NC_000023.10:g.110576321T>A
CLNSRC
CLNACC	RCV000145889.1,