{{Rsnum
|rsid=9640663
|Gene=PTPN12
|Chromosome=7
|position=77618504
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|GMAF=0.2392
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=PTPN12
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 39.3 | 47.3 | 13.4
| HCB | 77.4 | 19.7 | 2.9
| JPT | 88.5 | 11.5 | 0.0
| YRI | 78.9 | 20.4 | 0.7
| ASW | 71.9 | 26.3 | 1.8
| CHB | 77.4 | 19.7 | 2.9
| CHD | 74.8 | 24.3 | 0.9
| GIH | 47.5 | 44.6 | 7.9
| LWK | 77.3 | 21.8 | 0.9
| MEX | 65.5 | 27.6 | 6.9
| MKK | 65.4 | 30.1 | 4.5
| TSI | 38.2 | 52.9 | 8.8
| HapMapRevision=28
}}{{Venter SNP
|rsid=9640663
|allele=A
|frequency=0.367
|uid=1103652618557
|type=heterozygous_SNP
|hugo=PTPN12
|ensembl gene=ENSG00000127947
|ensembl transcript=ENST00000248594
|sift=TOLERATED
|disease=Defects in PTPN12 are found in some colon cancers.
}}

{{GET Evidence
|gene=PTPN12
|aa_change=Val322Ile
|aa_change_short=V322I
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs9640663
|overall_frequency_n=7210
|overall_frequency_d=10758
|overall_frequency=0.670199
|n_genomes=51
|n_genomes_annotated=0
|n_haplomes=85
|n_articles=0
|n_articles_annotated=0
|nblosum100=-4
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | Illumina Human 1M}}