rs869025590

Orientation

plus

Stabilized

plus

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

Make rs869025590(-;A)

Make rs869025590(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

41170002

Gene

USP9X

is a	snp
is	mentioned by
dbSNP	rs869025590
dbSNP (classic)	rs869025590
ClinGen	rs869025590
ebi	rs869025590
HLI	rs869025590
Exac	rs869025590
Gnomad	rs869025590
Varsome	rs869025590
LitVar	rs869025590
Map	rs869025590
PheGenI	rs869025590
Biobank	rs869025590
1000 genomes	rs869025590
hgdp	rs869025590
ensembl	rs869025590
geneview	rs869025590
scholar	rs869025590
google	rs869025590
pharmgkb	rs869025590
gwascentral	rs869025590
openSNP	rs869025590
23andMe	rs869025590
SNPshot	rs869025590
SNPdbe	rs869025590
MSV3d	rs869025590
GWAS Ctlg	rs869025590

Max Magnitude

0

ClinVar
Risk	rs869025590(A;A)
Alt	rs869025590(A;A)
Reference	Rs869025590(-;-)
Significance	Pathogenic
Disease	Mental retardation
Variation	info
Gene	USP9X
CLNDBN	Mental retardation, X-linked 99, syndromic, female-restricted
Reversed	0
HGVS	NC_000023.10:g.41029255_41029256insA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000208730.1,