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rs1064795335

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
ChromosomeX
Position41214594
GeneUSP9X
is asnp
is mentioned by
dbSNPrs1064795335
dbSNP (old)rs1064795335
ClinGenrs1064795335
ebirs1064795335
HLIrs1064795335
Exacrs1064795335
Gnomadrs1064795335
Varsomers1064795335
Maprs1064795335
PheGenIrs1064795335
Biobankrs1064795335
1000 genomesrs1064795335
hgdprs1064795335
ensemblrs1064795335
gopubmedrs1064795335
geneviewrs1064795335
scholarrs1064795335
googlers1064795335
pharmgkbrs1064795335
gwascentralrs1064795335
openSNPrs1064795335
23andMers1064795335
23andMe allrs1064795335
SNPshotrs1064795335
SNPdbers1064795335
MSV3drs1064795335
GWAS Ctlgrs1064795335
Max Magnitude0
ClinVar
Risk rs1064795335(A;A)
Alt rs1064795335(A;A)
Reference Rs1064795335(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene USP9X
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.41073847C>A
CLNSRC
CLNACC RCV000483949.1,