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rs587777317

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587777317(A;A)
Make rs587777317(A;T)
ReferenceGRCh38 38.1/142
ChromosomeX
Position41218440
GeneUSP9X
is asnp
is mentioned by
dbSNPrs587777317
ebirs587777317
HLIrs587777317
Exacrs587777317
Varsomers587777317
Maprs587777317
PheGenIrs587777317
hapmaprs587777317
1000 genomesrs587777317
hgdprs587777317
ensemblrs587777317
gopubmedrs587777317
geneviewrs587777317
scholarrs587777317
googlers587777317
pharmgkbrs587777317
gwascentralrs587777317
openSNPrs587777317
23andMers587777317
23andMe allrs587777317
SNP Nexus

SNPshotrs587777317
SNPdbers587777317
MSV3drs587777317
GWAS Ctlgrs587777317
Max Magnitude0
ClinVar
Risk rs587777317(A;A)
Alt rs587777317(A;A)
Reference rs587777317(T;T)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene USP9X
CLNDBN Mental retardation, X-linked 99
Reversed 0
HGVS NC_000023.10:g.41077693T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000114949.2,