rs797045519

Orientation

minus

Stabilized

minus

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

Make rs797045519(-;TAGCC)

Make rs797045519(TAGCC;TAGCC)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

111410313

Gene

DCX

is a	snp
is	mentioned by
dbSNP	rs797045519
dbSNP (classic)	rs797045519
ClinGen	rs797045519
ebi	rs797045519
HLI	rs797045519
Exac	rs797045519
Gnomad	rs797045519
Varsome	rs797045519
LitVar	rs797045519
Map	rs797045519
PheGenI	rs797045519
Biobank	rs797045519
1000 genomes	rs797045519
hgdp	rs797045519
ensembl	rs797045519
geneview	rs797045519
scholar	rs797045519
google	rs797045519
pharmgkb	rs797045519
gwascentral	rs797045519
openSNP	rs797045519
23andMe	rs797045519
SNPshot	rs797045519
SNPdbe	rs797045519
MSV3d	rs797045519
GWAS Ctlg	rs797045519

Max Magnitude

0

ClinVar
Risk	rs797045519(TAGCC;TAGCC)
Alt	rs797045519(TAGCC;TAGCC)
Reference	Rs797045519(-;-)
Significance	Pathogenic
Disease	Abnormal cortical gyration
Variation	info
Gene	DCX
CLNDBN	Abnormal cortical gyration
Reversed	1
HGVS	NC_000023.10:g.110653542_110653546dupGGCTA
CLNSRC
CLNACC	RCV000193837.1,