rs587783096

Orientation

minus

Stabilized

minus

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

Make rs587783096(A;A)

Make rs587783096(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

25007418

Gene

ARX

is a	snp
is	mentioned by
dbSNP	rs587783096
dbSNP (classic)	rs587783096
ClinGen	rs587783096
ebi	rs587783096
HLI	rs587783096
Exac	rs587783096
Gnomad	rs587783096
Varsome	rs587783096
LitVar	rs587783096
Map	rs587783096
PheGenI	rs587783096
Biobank	rs587783096
1000 genomes	rs587783096
hgdp	rs587783096
ensembl	rs587783096
geneview	rs587783096
scholar	rs587783096
google	rs587783096
pharmgkb	rs587783096
gwascentral	rs587783096
openSNP	rs587783096
23andMe	rs587783096
SNPshot	rs587783096
SNPdbe	rs587783096
MSV3d	rs587783096
GWAS Ctlg	rs587783096

Max Magnitude

0

ClinVar
Risk	rs587783096(A;A)
Alt	rs587783096(A;A)
Reference	Rs587783096(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	ARX
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.25025535C>T
CLNSRC
CLNACC	RCV000144762.2,