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rs869025589

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869025589(A;G)
Make rs869025589(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position41171836
GeneUSP9X
is asnp
is mentioned by
dbSNPrs869025589
ClinGenrs869025589
ebirs869025589
HLIrs869025589
Exacrs869025589
Varsomers869025589
Maprs869025589
PheGenIrs869025589
hapmaprs869025589
1000 genomesrs869025589
hgdprs869025589
ensemblrs869025589
gopubmedrs869025589
geneviewrs869025589
scholarrs869025589
googlers869025589
pharmgkbrs869025589
gwascentralrs869025589
openSNPrs869025589
23andMers869025589
23andMe allrs869025589
SNP Nexus

SNPshotrs869025589
SNPdbers869025589
MSV3drs869025589
GWAS Ctlgrs869025589
Max Magnitude0
ClinVar
Risk rs869025589(G;G)
Alt rs869025589(G;G)
Reference Rs869025589(A;A)
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.41031089A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000208717.1,