rs587783585

Orientation

minus

Stabilized

minus

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

Make rs587783585(G;T)

Make rs587783585(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

111333108

Gene

DCX

is a	snp
is	mentioned by
dbSNP	rs587783585
dbSNP (classic)	rs587783585
ClinGen	rs587783585
ebi	rs587783585
HLI	rs587783585
Exac	rs587783585
Gnomad	rs587783585
Varsome	rs587783585
LitVar	rs587783585
Map	rs587783585
PheGenI	rs587783585
Biobank	rs587783585
1000 genomes	rs587783585
hgdp	rs587783585
ensembl	rs587783585
geneview	rs587783585
scholar	rs587783585
google	rs587783585
pharmgkb	rs587783585
gwascentral	rs587783585
openSNP	rs587783585
23andMe	rs587783585
SNPshot	rs587783585
SNPdbe	rs587783585
MSV3d	rs587783585
GWAS Ctlg	rs587783585

Max Magnitude

0

ClinVar
Risk	rs587783585(T;T)
Alt	rs587783585(T;T)
Reference	Rs587783585(G;G)
Significance	Pathogenic
Disease	Heterotopia
Variation	info
Gene	DCX
CLNDBN	Heterotopia
Reversed	1
HGVS	NC_000023.10:g.110576336C>A
CLNSRC
CLNACC	RCV000145888.1,