rs267606666

Orientation

minus

Stabilized

minus

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

Make rs267606666(G;T)

Make rs267606666(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

25013763

Gene

ARX

is a	snp
is	mentioned by
dbSNP	rs267606666
dbSNP (classic)	rs267606666
ClinGen	rs267606666
ebi	rs267606666
HLI	rs267606666
Exac	rs267606666
Gnomad	rs267606666
Varsome	rs267606666
LitVar	rs267606666
Map	rs267606666
PheGenI	rs267606666
Biobank	rs267606666
1000 genomes	rs267606666
hgdp	rs267606666
ensembl	rs267606666
geneview	rs267606666
scholar	rs267606666
google	rs267606666
pharmgkb	rs267606666
gwascentral	rs267606666
openSNP	rs267606666
23andMe	rs267606666
SNPshot	rs267606666
SNPdbe	rs267606666
MSV3d	rs267606666
GWAS Ctlg	rs267606666

Max Magnitude

0

ClinVar
Risk	rs267606666(T;T)
Alt	rs267606666(T;T)
Reference	Rs267606666(G;G)
Significance	Pathogenic
Disease	Lissencephaly 2
Variation	info
Gene	ARX
CLNDBN	Lissencephaly 2, X-linked
Reversed	1
HGVS	NC_000023.10:g.25031880C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011956.8,