rs104894784

Orientation

minus

Stabilized

minus

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

Make rs104894784(A;A)

Make rs104894784(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

111410166

Gene

DCX

is a	snp
is	mentioned by
dbSNP	rs104894784
dbSNP (classic)	rs104894784
ClinGen	rs104894784
ebi	rs104894784
HLI	rs104894784
Exac	rs104894784
Gnomad	rs104894784
Varsome	rs104894784
LitVar	rs104894784
Map	rs104894784
PheGenI	rs104894784
Biobank	rs104894784
1000 genomes	rs104894784
hgdp	rs104894784
ensembl	rs104894784
geneview	rs104894784
scholar	rs104894784
google	rs104894784
pharmgkb	rs104894784
gwascentral	rs104894784
openSNP	rs104894784
23andMe	rs104894784
SNPshot	rs104894784
SNPdbe	rs104894784
MSV3d	rs104894784
GWAS Ctlg	rs104894784

Max Magnitude

0

OMIM	300121
Desc
Variant	0011
Related	also

ClinVar
Risk	rs104894784(A;A) rs104894784(T;T)
Alt	rs104894784(A;A) rs104894784(T;T)
Reference	Rs104894784(G;G)
Significance	Pathogenic
Disease	Heterotopia Subcortical laminar heterotopia
Variation	info
Gene	DCX
CLNDBN	Heterotopia Subcortical laminar heterotopia, X-linked
Reversed	1
HGVS	NC_000023.10:g.110653394C>A; NC_000023.10:g.110653394C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000145824.1, RCV000012371.24,