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rs1064795608

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
ChromosomeX
Position41143432
GeneUSP9X
is asnp
is mentioned by
dbSNPrs1064795608
dbSNP (old)rs1064795608
ClinGenrs1064795608
ebirs1064795608
HLIrs1064795608
Exacrs1064795608
Gnomadrs1064795608
Varsomers1064795608
Maprs1064795608
PheGenIrs1064795608
Biobankrs1064795608
1000 genomesrs1064795608
hgdprs1064795608
ensemblrs1064795608
gopubmedrs1064795608
geneviewrs1064795608
scholarrs1064795608
googlers1064795608
pharmgkbrs1064795608
gwascentralrs1064795608
openSNPrs1064795608
23andMers1064795608
23andMe allrs1064795608
SNPshotrs1064795608
SNPdbers1064795608
MSV3drs1064795608
GWAS Ctlgrs1064795608
Max Magnitude0
ClinVar
Risk rs1064795608(C;C)
Alt rs1064795608(C;C)
Reference Rs1064795608(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene USP9X
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.41002685T>C
CLNSRC
CLNACC RCV000482190.1,