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rs1064796854

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
ChromosomeX
Position41229398
GeneUSP9X
is asnp
is mentioned by
dbSNPrs1064796854
dbSNP (old)rs1064796854
ClinGenrs1064796854
ebirs1064796854
HLIrs1064796854
Exacrs1064796854
Gnomadrs1064796854
Varsomers1064796854
Maprs1064796854
PheGenIrs1064796854
Biobankrs1064796854
1000 genomesrs1064796854
hgdprs1064796854
ensemblrs1064796854
gopubmedrs1064796854
geneviewrs1064796854
scholarrs1064796854
googlers1064796854
pharmgkbrs1064796854
gwascentralrs1064796854
openSNPrs1064796854
23andMers1064796854
23andMe allrs1064796854
SNPshotrs1064796854
SNPdbers1064796854
MSV3drs1064796854
GWAS Ctlgrs1064796854
Max Magnitude0
ClinVar
Risk rs1064796854(T;T)
Alt rs1064796854(T;T)
Reference Rs1064796854(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene USP9X
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.41088651C>T
CLNSRC
CLNACC RCV000480003.1,