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rs1085307914

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
ChromosomeX
Position41134794
GeneUSP9X
is asnp
is mentioned by
dbSNPrs1085307914
dbSNP (old)rs1085307914
ClinGenrs1085307914
ebirs1085307914
HLIrs1085307914
Exacrs1085307914
Gnomadrs1085307914
Varsomers1085307914
Maprs1085307914
PheGenIrs1085307914
Biobankrs1085307914
1000 genomesrs1085307914
hgdprs1085307914
ensemblrs1085307914
gopubmedrs1085307914
geneviewrs1085307914
scholarrs1085307914
googlers1085307914
pharmgkbrs1085307914
gwascentralrs1085307914
openSNPrs1085307914
23andMers1085307914
23andMe allrs1085307914
SNPshotrs1085307914
SNPdbers1085307914
MSV3drs1085307914
GWAS Ctlgrs1085307914
Max Magnitude0
ClinVar
Risk rs1085307914(A;A)
Alt rs1085307914(A;A)
Reference Rs1085307914(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene USP9X
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.40994047T>A
CLNSRC
CLNACC RCV000489858.1,