{{Rsnum
|rsid=9899177
|Gene=USP6
|Chromosome=17
|position=5155513
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|GMAF=0.3972
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=USP6
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 45.5 | 37.5 | 17.0
| HCB | 2.2 | 30.1 | 67.6
| JPT | 0.0 | 16.8 | 83.2
| YRI | 4.8 | 29.3 | 66.0
| ASW | 5.3 | 38.6 | 56.1
| CHB | 2.2 | 30.1 | 67.6
| CHD | 3.7 | 28.7 | 67.6
| GIH | 4.0 | 39.6 | 56.4
| LWK | 1.8 | 32.7 | 65.5
| MEX | 31.0 | 51.7 | 17.2
| MKK | 8.4 | 41.6 | 50.0
| TSI | 45.1 | 40.2 | 14.7
| HapMapRevision=28
}}

{{Venter SNP
|rsid=9899177
|allele=A
|frequency=0.333
|uid=1103645267693
|type=heterozygous_SNP
|hugo=USP6
|ensembl gene=ENSG00000129204
|ensembl transcript=ENST00000250066
|sift=TOLERATED
|disease=Involved in tumorigenesis.
}}

{{GET Evidence
|gene=USP6
|aa_change=Arg912Gln
|aa_change_short=R912Q
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs9899177
|overall_frequency_n=5583
|overall_frequency_d=10758
|overall_frequency=0.518963
|n_genomes=30
|n_genomes_annotated=0
|n_haplomes=39
|n_articles=0
|n_articles_annotated=0
|pph2_score=0.975
|nblosum100=0
|autoscore=1
|webscore=N
}}
{{on chip | 23andMe v3}}
{{on chip | FTDNA2}}
{{on chip | Illumina Human 1M}}