rs587783548

Orientation

minus

Stabilized

minus

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

Make rs587783548(C;T)

Make rs587783548(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

111401309

Gene

DCX

is a	snp
is	mentioned by
dbSNP	rs587783548
dbSNP (classic)	rs587783548
ClinGen	rs587783548
ebi	rs587783548
HLI	rs587783548
Exac	rs587783548
Gnomad	rs587783548
Varsome	rs587783548
LitVar	rs587783548
Map	rs587783548
PheGenI	rs587783548
Biobank	rs587783548
1000 genomes	rs587783548
hgdp	rs587783548
ensembl	rs587783548
geneview	rs587783548
scholar	rs587783548
google	rs587783548
pharmgkb	rs587783548
gwascentral	rs587783548
openSNP	rs587783548
23andMe	rs587783548
SNPshot	rs587783548
SNPdbe	rs587783548
MSV3d	rs587783548
GWAS Ctlg	rs587783548

Max Magnitude

0

ClinVar
Risk	rs587783548(T;T)
Alt	rs587783548(T;T)
Reference	Rs587783548(C;C)
Significance	Pathogenic
Disease	Heterotopia
Variation	info
Gene	DCX
CLNDBN	Heterotopia
Reversed	1
HGVS	NC_000023.10:g.110644537G>A
CLNSRC
CLNACC	RCV000145842.1,