{{Rsnum
|rsid=8073787
|Gene=USP6
|Chromosome=17
|position=5139599
|Orientation=plus
|ReferenceAllele=T
|MissenseAllele=C
|GMAF=0.275
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=USP6
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 27.8 | 47.2 | 25.0
| HCB | 80.0 | 20.0 | 0.0
| JPT | 92.9 | 7.1 | 0.0
| YRI | 72.1 | 27.1 | 0.7
| ASW | 0.0 | 0.0 | 0.0
| CHB | 80.0 | 20.0 | 0.0
| CHD | 75.0 | 23.1 | 1.9
| GIH | 66.0 | 32.0 | 2.0
| LWK | 76.2 | 23.8 | 0.0
| MEX | 37.5 | 46.4 | 16.1
| MKK | 74.0 | 26.0 | 0.0
| TSI | 25.5 | 46.9 | 27.6
| HapMapRevision=28
}}

{{Venter SNP
|rsid=8073787
|allele=C
|frequency=0.492
|uid=1103645267659
|type=heterozygous_SNP
|hugo=USP6
|ensembl gene=ENSG00000129204
|ensembl transcript=ENST00000250066
|sift=TOLERATED
|disease=Involved in tumorigenesis.
}}

{{GET Evidence
|gene=USP6
|aa_change=Trp475Arg
|aa_change_short=W475R
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs8073787
|overall_frequency_n=6858
|overall_frequency_d=10758
|overall_frequency=0.637479
|n_genomes=49
|n_genomes_annotated=0
|n_haplomes=81
|n_articles=0
|n_articles_annotated=0
|nblosum100=7
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}