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rs869025591

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869025591(C;T)
Make rs869025591(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position41188070
GeneUSP9X
is asnp
is mentioned by
dbSNPrs869025591
ebirs869025591
HLIrs869025591
Exacrs869025591
Varsomers869025591
Maprs869025591
PheGenIrs869025591
hapmaprs869025591
1000 genomesrs869025591
hgdprs869025591
ensemblrs869025591
gopubmedrs869025591
geneviewrs869025591
scholarrs869025591
googlers869025591
pharmgkbrs869025591
gwascentralrs869025591
openSNPrs869025591
23andMers869025591
23andMe allrs869025591
SNP Nexus

SNPshotrs869025591
SNPdbers869025591
MSV3drs869025591
GWAS Ctlgrs869025591
Max Magnitude0
ClinVar
Risk rs869025591(T;T)
Alt rs869025591(T;T)
Reference rs869025591(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.41047323C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000208740.1,