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

rs869025592

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869025592(C;T)
Make rs869025592(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position41141381
GeneUSP9X
is asnp
is mentioned by
dbSNPrs869025592
ebirs869025592
HLIrs869025592
Exacrs869025592
Varsomers869025592
Maprs869025592
PheGenIrs869025592
hapmaprs869025592
1000 genomesrs869025592
hgdprs869025592
ensemblrs869025592
gopubmedrs869025592
geneviewrs869025592
scholarrs869025592
googlers869025592
pharmgkbrs869025592
gwascentralrs869025592
openSNPrs869025592
23andMers869025592
23andMe allrs869025592
SNP Nexus

SNPshotrs869025592
SNPdbers869025592
MSV3drs869025592
GWAS Ctlgrs869025592
Max Magnitude0
ClinVar
Risk rs869025592(T;T)
Alt rs869025592(T;T)
Reference rs869025592(C;C)
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.41000634C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000208723.1,