rs587783182

Orientation

minus

Stabilized

minus

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

Make rs587783182(C;T)

Make rs587783182(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

25010268

Gene

ARX

is a	snp
is	mentioned by
dbSNP	rs587783182
dbSNP (classic)	rs587783182
ClinGen	rs587783182
ebi	rs587783182
HLI	rs587783182
Exac	rs587783182
Gnomad	rs587783182
Varsome	rs587783182
LitVar	rs587783182
Map	rs587783182
PheGenI	rs587783182
Biobank	rs587783182
1000 genomes	rs587783182
hgdp	rs587783182
ensembl	rs587783182
geneview	rs587783182
scholar	rs587783182
google	rs587783182
pharmgkb	rs587783182
gwascentral	rs587783182
openSNP	rs587783182
23andMe	rs587783182
SNPshot	rs587783182
SNPdbe	rs587783182
MSV3d	rs587783182
GWAS Ctlg	rs587783182

Max Magnitude

0

ClinVar
Risk	rs587783182(T;T)
Alt	rs587783182(T;T)
Reference	Rs587783182(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	ARX
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.25028385G>A
CLNSRC
CLNACC	RCV000145038.1,