rs797045291

Orientation

minus

Stabilized

minus

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

Make rs797045291(-;C)

Make rs797045291(C;C)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

25007221

Gene

ARX

is a	snp
is	mentioned by
dbSNP	rs797045291
dbSNP (classic)	rs797045291
ClinGen	rs797045291
ebi	rs797045291
HLI	rs797045291
Exac	rs797045291
Gnomad	rs797045291
Varsome	rs797045291
LitVar	rs797045291
Map	rs797045291
PheGenI	rs797045291
Biobank	rs797045291
1000 genomes	rs797045291
hgdp	rs797045291
ensembl	rs797045291
geneview	rs797045291
scholar	rs797045291
google	rs797045291
pharmgkb	rs797045291
gwascentral	rs797045291
openSNP	rs797045291
23andMe	rs797045291
SNPshot	rs797045291
SNPdbe	rs797045291
MSV3d	rs797045291
GWAS Ctlg	rs797045291

Max Magnitude

0

ClinVar
Risk	rs797045291(C;C)
Alt	rs797045291(C;C)
Reference	Rs797045291(-;-)
Significance	Pathogenic
Disease	Lissencephaly 2
Variation	info
Gene	ARX
CLNDBN	Lissencephaly 2, X-linked
Reversed	1
HGVS	NC_000023.10:g.25025339dupG
CLNSRC
CLNACC	RCV000193341.1,