rs797045515

Orientation

minus

Stabilized

minus

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

Make rs797045515(-;-)

Make rs797045515(-;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

111401169

Gene

DCX

is a	snp
is	mentioned by
dbSNP	rs797045515
dbSNP (classic)	rs797045515
ClinGen	rs797045515
ebi	rs797045515
HLI	rs797045515
Exac	rs797045515
Gnomad	rs797045515
Varsome	rs797045515
LitVar	rs797045515
Map	rs797045515
PheGenI	rs797045515
Biobank	rs797045515
1000 genomes	rs797045515
hgdp	rs797045515
ensembl	rs797045515
geneview	rs797045515
scholar	rs797045515
google	rs797045515
pharmgkb	rs797045515
gwascentral	rs797045515
openSNP	rs797045515
23andMe	rs797045515
SNPshot	rs797045515
SNPdbe	rs797045515
MSV3d	rs797045515
GWAS Ctlg	rs797045515

Max Magnitude

0

ClinVar
Risk	rs797045515(-;-)
Alt	rs797045515(-;-)
Reference	Rs797045515(T;T)
Significance	Pathogenic
Disease	Abnormal cortical gyration
Variation	info
Gene	DCX
CLNDBN	Abnormal cortical gyration
Reversed	1
HGVS	NC_000023.10:g.110644397delA
CLNSRC
CLNACC	RCV000192741.1,