rs201870761

Orientation

plus

Stabilized

plus

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

Make rs201870761(C;C)

Make rs201870761(C;T)

Reference

GRCh38 38.1/142

Chromosome

X

Position

111410089

Gene

DCX

is a	snp
is	mentioned by
dbSNP	rs201870761
dbSNP (classic)	rs201870761
ClinGen	rs201870761
ebi	rs201870761
HLI	rs201870761
Exac	rs201870761
Gnomad	rs201870761
Varsome	rs201870761
LitVar	rs201870761
Map	rs201870761
PheGenI	rs201870761
Biobank	rs201870761
1000 genomes	rs201870761
hgdp	rs201870761
ensembl	rs201870761
geneview	rs201870761
scholar	rs201870761
google	rs201870761
pharmgkb	rs201870761
gwascentral	rs201870761
openSNP	rs201870761
23andMe	rs201870761
SNPshot	rs201870761
SNPdbe	rs201870761
MSV3d	rs201870761
GWAS Ctlg	rs201870761

Max Magnitude

0

ClinVar
Risk	rs201870761(A;A) rs201870761(C;C)
Alt	rs201870761(A;A) rs201870761(C;C)
Reference	Rs201870761(T;T)
Significance	Pathogenic
Disease	Heterotopia
Variation	info
Gene	DCX
CLNDBN	Heterotopia
Reversed	0
HGVS	NC_000023.10:g.110653317T>A
CLNSRC	ClinVar University of Chicago
CLNACC	RCV000145835.1,