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rs869025588

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869025588(C;T)
Make rs869025588(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position41168136
GeneUSP9X
is asnp
is mentioned by
dbSNPrs869025588
ebirs869025588
HLIrs869025588
Exacrs869025588
Varsomers869025588
Maprs869025588
PheGenIrs869025588
hapmaprs869025588
1000 genomesrs869025588
hgdprs869025588
ensemblrs869025588
gopubmedrs869025588
geneviewrs869025588
scholarrs869025588
googlers869025588
pharmgkbrs869025588
gwascentralrs869025588
openSNPrs869025588
23andMers869025588
23andMe allrs869025588
SNP Nexus

SNPshotrs869025588
SNPdbers869025588
MSV3drs869025588
GWAS Ctlgrs869025588
Max Magnitude0
ClinVar
Risk rs869025588(T;T)
Alt rs869025588(T;T)
Reference rs869025588(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.41027389C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000208736.1,