Have questions? Visit https://www.reddit.com/r/SNPedia

rs869025590

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs869025590(-;-)
Make rs869025590(-;A)
Make rs869025590(A;A)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position41170002
GeneUSP9X
is asnp
is mentioned by
dbSNPrs869025590
ebirs869025590
HLIrs869025590
Exacrs869025590
Varsomers869025590
Maprs869025590
PheGenIrs869025590
hapmaprs869025590
1000 genomesrs869025590
hgdprs869025590
ensemblrs869025590
gopubmedrs869025590
geneviewrs869025590
scholarrs869025590
googlers869025590
pharmgkbrs869025590
gwascentralrs869025590
openSNPrs869025590
23andMers869025590
23andMe allrs869025590
SNP Nexus

SNPshotrs869025590
SNPdbers869025590
MSV3drs869025590
GWAS Ctlgrs869025590
Max Magnitude0
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,