rs587783549

Orientation

minus

Stabilized

minus

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

Make rs587783549(-;-)

Make rs587783549(-;AAC)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

111401302

Gene

DCX

is a	snp
is	mentioned by
dbSNP	rs587783549
dbSNP (classic)	rs587783549
ClinGen	rs587783549
ebi	rs587783549
HLI	rs587783549
Exac	rs587783549
Gnomad	rs587783549
Varsome	rs587783549
LitVar	rs587783549
Map	rs587783549
PheGenI	rs587783549
Biobank	rs587783549
1000 genomes	rs587783549
hgdp	rs587783549
ensembl	rs587783549
geneview	rs587783549
scholar	rs587783549
google	rs587783549
pharmgkb	rs587783549
gwascentral	rs587783549
openSNP	rs587783549
23andMe	rs587783549
SNPshot	rs587783549
SNPdbe	rs587783549
MSV3d	rs587783549
GWAS Ctlg	rs587783549

Max Magnitude

0

ClinVar
Risk	rs587783549(-;-)
Alt	rs587783549(-;-)
Reference	Rs587783549(AAC;AAC)
Significance	Pathogenic
Disease	Heterotopia
Variation	info
Gene	DCX
CLNDBN	Heterotopia
Reversed	1
HGVS	NC_000023.10:g.110644530_110644532delGTT
CLNSRC
CLNACC	RCV000145843.1,