{{Rsnum
|rsid=1503185
|Gene=PTPRJ
|Chromosome=11
|position=48125070
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=A
|GMAF=0.2172
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=PTPRJ
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 77.0 | 21.2 | 1.8
| HCB | 67.9 | 25.5 | 6.6
| JPT | 54.9 | 40.7 | 4.4
| YRI | 53.1 | 37.4 | 9.5
| ASW | 43.9 | 45.6 | 10.5
| CHB | 67.9 | 25.5 | 6.6
| CHD | 53.2 | 41.3 | 5.5
| GIH | 56.4 | 36.6 | 6.9
| LWK | 45.5 | 45.5 | 9.1
| MEX | 77.6 | 20.7 | 1.7
| MKK | 55.1 | 39.1 | 5.8
| TSI | 54.9 | 38.2 | 6.9
| HapMapRevision=28
}}{{Venter SNP
|rsid=1503185
|allele=A
|frequency=0.133
|uid=1103649680132
|type=heterozygous_SNP
|hugo=PTPRJ
|ensembl gene=ENSG00000149177
|ensembl transcript=ENST00000278456
|sift=TOLERATED
|disease=Defects in PTPRJ are found in cancers of colon, lung, and breast.
}}

{{PMID Auto
|PMID=18843023
|Title=PTPRJ haplotypes and colorectal cancer risk.
}}

{{GET Evidence
|gene=PTPRJ
|aa_change=Arg326Gln
|aa_change_short=R326Q
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1503185
|overall_frequency_n=2112
|overall_frequency_d=10758
|overall_frequency=0.196319
|n_genomes=17
|n_genomes_annotated=0
|n_haplomes=22
|n_articles=0
|n_articles_annotated=0
|pph2_score=0.004
|nblosum100=0
|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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}