rs587783541

Orientation

minus

Stabilized

minus

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

Make rs587783541(C;T)

Make rs587783541(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

111410095

Gene

DCX

is a	snp
is	mentioned by
dbSNP	rs587783541
dbSNP (classic)	rs587783541
ClinGen	rs587783541
ebi	rs587783541
HLI	rs587783541
Exac	rs587783541
Gnomad	rs587783541
Varsome	rs587783541
LitVar	rs587783541
Map	rs587783541
PheGenI	rs587783541
Biobank	rs587783541
1000 genomes	rs587783541
hgdp	rs587783541
ensembl	rs587783541
geneview	rs587783541
scholar	rs587783541
google	rs587783541
pharmgkb	rs587783541
gwascentral	rs587783541
openSNP	rs587783541
23andMe	rs587783541
SNPshot	rs587783541
SNPdbe	rs587783541
MSV3d	rs587783541
GWAS Ctlg	rs587783541

Max Magnitude

0

ClinVar
Risk	rs587783541(G;G) rs587783541(T;T)
Alt	rs587783541(G;G) rs587783541(T;T)
Reference	Rs587783541(C;C)
Significance	Pathogenic
Disease	Heterotopia not provided
Variation	info
Gene	DCX
CLNDBN	Heterotopia not provided
Reversed	1
HGVS	NC_000023.10:g.110653323G>A; NC_000023.10:g.110653323G>C
CLNSRC
CLNACC	RCV000145833.1, RCV000377977.1,