rs587783568

Orientation

minus

Stabilized

minus

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

Make rs587783568(A;A)

Make rs587783568(A;C)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

111401109

Gene

DCX

is a	snp
is	mentioned by
dbSNP	rs587783568
dbSNP (classic)	rs587783568
ClinGen	rs587783568
ebi	rs587783568
HLI	rs587783568
Exac	rs587783568
Gnomad	rs587783568
Varsome	rs587783568
LitVar	rs587783568
Map	rs587783568
PheGenI	rs587783568
Biobank	rs587783568
1000 genomes	rs587783568
hgdp	rs587783568
ensembl	rs587783568
geneview	rs587783568
scholar	rs587783568
google	rs587783568
pharmgkb	rs587783568
gwascentral	rs587783568
openSNP	rs587783568
23andMe	rs587783568
SNPshot	rs587783568
SNPdbe	rs587783568
MSV3d	rs587783568
GWAS Ctlg	rs587783568

Max Magnitude

0

ClinVar
Risk	rs587783568(A;A) rs587783568(G;G) rs587783568(T;T)
Alt	rs587783568(A;A) rs587783568(G;G) rs587783568(T;T)
Reference	Rs587783568(C;C)
Significance	Pathogenic
Disease	Heterotopia not provided
Variation	info
Gene	DCX
CLNDBN	Heterotopia not provided
Reversed	1
HGVS	NC_000023.10:g.110644337G>A; NC_000023.10:g.110644337G>C; NC_000023.10:g.110644337G>T
CLNSRC
CLNACC	RCV000145868.1, RCV000440789.1, RCV000145867.1, RCV000145866.1,