rs1064793735

Orientation

minus

Stabilized

minus

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

Chromosome

X

Position

111410034

Gene

DCX

is a	snp
is	mentioned by
dbSNP	rs1064793735
dbSNP (classic)	rs1064793735
ClinGen	rs1064793735
ebi	rs1064793735
HLI	rs1064793735
Exac	rs1064793735
Gnomad	rs1064793735
Varsome	rs1064793735
LitVar	rs1064793735
Map	rs1064793735
PheGenI	rs1064793735
Biobank	rs1064793735
1000 genomes	rs1064793735
hgdp	rs1064793735
ensembl	rs1064793735
geneview	rs1064793735
scholar	rs1064793735
google	rs1064793735
pharmgkb	rs1064793735
gwascentral	rs1064793735
openSNP	rs1064793735
23andMe	rs1064793735
SNPshot	rs1064793735
SNPdbe	rs1064793735
MSV3d	rs1064793735
GWAS Ctlg	rs1064793735

Max Magnitude

0

ClinVar
Risk	rs1064793735(-;-)
Alt	rs1064793735(-;-)
Reference	Rs1064793735(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	DCX
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.110653262delC
CLNSRC
CLNACC	RCV000478400.1,