rs104894779

Orientation

minus

Stabilized

minus

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

Make rs104894779(A;A)

Make rs104894779(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

111410215

Gene

DCX

is a	snp
is	mentioned by
dbSNP	rs104894779
dbSNP (classic)	rs104894779
ClinGen	rs104894779
ebi	rs104894779
HLI	rs104894779
Exac	rs104894779
Gnomad	rs104894779
Varsome	rs104894779
LitVar	rs104894779
Map	rs104894779
PheGenI	rs104894779
Biobank	rs104894779
1000 genomes	rs104894779
hgdp	rs104894779
ensembl	rs104894779
geneview	rs104894779
scholar	rs104894779
google	rs104894779
pharmgkb	rs104894779
gwascentral	rs104894779
openSNP	rs104894779
23andMe	rs104894779
SNPshot	rs104894779
SNPdbe	rs104894779
MSV3d	rs104894779
GWAS Ctlg	rs104894779

Max Magnitude

0

OMIM	300121
Desc
Variant	0001
Related	also

ClinVar
Risk	rs104894779(A;A)
Alt	rs104894779(A;A)
Reference	Rs104894779(G;G)
Significance	Pathogenic
Disease	Lissencephaly Subcortical laminar heterotopia
Variation	info
Gene	DCX
CLNDBN	Lissencephaly, X-linked Subcortical laminar heterotopia, X-linked
Reversed	1
HGVS	NC_000023.10:g.110653443C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000012355.16, RCV000012356.24,