rs886039308

Orientation

minus

Stabilized

minus

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

Make rs886039308(A;A)

Make rs886039308(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

X

Position

25013006

Gene

ARX

is a	snp
is	mentioned by
dbSNP	rs886039308
dbSNP (classic)	rs886039308
ClinGen	rs886039308
ebi	rs886039308
HLI	rs886039308
Exac	rs886039308
Gnomad	rs886039308
Varsome	rs886039308
LitVar	rs886039308
Map	rs886039308
PheGenI	rs886039308
Biobank	rs886039308
1000 genomes	rs886039308
hgdp	rs886039308
ensembl	rs886039308
geneview	rs886039308
scholar	rs886039308
google	rs886039308
pharmgkb	rs886039308
gwascentral	rs886039308
openSNP	rs886039308
23andMe	rs886039308
SNPshot	rs886039308
SNPdbe	rs886039308
MSV3d	rs886039308
GWAS Ctlg	rs886039308

Max Magnitude

0

ClinVar
Risk	rs886039308(A;A)
Alt	rs886039308(A;A)
Reference	Rs886039308(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	ARX
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.25031123C>T
CLNSRC
CLNACC	RCV000255677.2,