rs398124511

Orientation

minus

Stabilized

minus

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

Make rs398124511(-;AGCCGCGGCCGCGGCCGCCGCGGC)

Make rs398124511(AGCCGCGGCCGCGGCCGCCGCGGC;AGCCGCGGCCGCGGCCGCCGCGGC)

Reference

GRCh38 38.1/141

Chromosome

X

Position

25013530

Gene

ARX

is a	snp
is	mentioned by
dbSNP	rs398124511
dbSNP (classic)	rs398124511
ClinGen	rs398124511
ebi	rs398124511
HLI	rs398124511
Exac	rs398124511
Gnomad	rs398124511
Varsome	rs398124511
LitVar	rs398124511
Map	rs398124511
PheGenI	rs398124511
Biobank	rs398124511
1000 genomes	rs398124511
hgdp	rs398124511
ensembl	rs398124511
geneview	rs398124511
scholar	rs398124511
google	rs398124511
pharmgkb	rs398124511
gwascentral	rs398124511
openSNP	rs398124511
23andMe	rs398124511
SNPshot	rs398124511
SNPdbe	rs398124511
MSV3d	rs398124511
GWAS Ctlg	rs398124511

Max Magnitude

0

ClinVar
Risk	rs398124511(AGCCGCGGCCGCGGCCGCCGCGGC;AGCCGCGGCCGCGGCCGCCGCGGC)
Alt	rs398124511(AGCCGCGGCCGCGGCCGCCGCGGC;AGCCGCGGCCGCGGCCGCCGCGGC)
Reference	Rs398124511(-;-)
Significance	Pathogenic
Disease	not provided Lissencephaly 2 Mental retardation
Variation	info
Gene	ARX
CLNDBN	not provided Lissencephaly 2, X-linked Mental retardation, with or without seizures, ARX-related, X-linked
Reversed	1
HGVS	NC_000023.10:g.25031648_25031671dup24
CLNSRC	HGMD
CLNACC	RCV000082605.4, RCV000192670.2, RCV000348945.1,