rs797045517

Orientation

minus

Stabilized

minus

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

Make rs797045517(-;A)

Make rs797045517(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

111401013

Gene

DCX

is a	snp
is	mentioned by
dbSNP	rs797045517
dbSNP (classic)	rs797045517
ClinGen	rs797045517
ebi	rs797045517
HLI	rs797045517
Exac	rs797045517
Gnomad	rs797045517
Varsome	rs797045517
LitVar	rs797045517
Map	rs797045517
PheGenI	rs797045517
Biobank	rs797045517
1000 genomes	rs797045517
hgdp	rs797045517
ensembl	rs797045517
geneview	rs797045517
scholar	rs797045517
google	rs797045517
pharmgkb	rs797045517
gwascentral	rs797045517
openSNP	rs797045517
23andMe	rs797045517
SNPshot	rs797045517
SNPdbe	rs797045517
MSV3d	rs797045517
GWAS Ctlg	rs797045517

Max Magnitude

0

ClinVar
Risk	rs797045517(A;A)
Alt	rs797045517(A;A)
Reference	Rs797045517(-;-)
Significance	Pathogenic
Disease	Abnormal cortical gyration
Variation	info
Gene	DCX
CLNDBN	Abnormal cortical gyration
Reversed	1
HGVS	NC_000023.10:g.110644242dupT
CLNSRC
CLNACC	RCV000195154.1,