rs797045292

Orientation

minus

Stabilized

minus

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

Make rs797045292(-;C)

Make rs797045292(C;C)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

25004887

Gene

ARX

is a	snp
is	mentioned by
dbSNP	rs797045292
dbSNP (classic)	rs797045292
ClinGen	rs797045292
ebi	rs797045292
HLI	rs797045292
Exac	rs797045292
Gnomad	rs797045292
Varsome	rs797045292
LitVar	rs797045292
Map	rs797045292
PheGenI	rs797045292
Biobank	rs797045292
1000 genomes	rs797045292
hgdp	rs797045292
ensembl	rs797045292
geneview	rs797045292
scholar	rs797045292
google	rs797045292
pharmgkb	rs797045292
gwascentral	rs797045292
openSNP	rs797045292
23andMe	rs797045292
SNPshot	rs797045292
SNPdbe	rs797045292
MSV3d	rs797045292
GWAS Ctlg	rs797045292

Max Magnitude

0

ClinVar
Risk	rs797045292(C;C)
Alt	rs797045292(C;C)
Reference	Rs797045292(-;-)
Significance	Pathogenic
Disease	Lissencephaly 2
Variation	info
Gene	ARX
CLNDBN	Lissencephaly 2, X-linked
Reversed	1
HGVS	NC_000023.10:g.25023005dupG
CLNSRC
CLNACC	RCV000195080.1,