{{Rsnum
|rsid=1130496
|Gene=PTPRN2
|Chromosome=7
|position=158167203
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=A
|GMAF=0.3526
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=PTPRN2
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 19.0 | 54.0 | 27.0
| HCB | 20.0 | 44.4 | 35.6
| JPT | 7.0 | 46.5 | 46.5
| YRI | 3.3 | 26.2 | 70.5
| ASW | 0.0 | 0.0 | 0.0
| CHB | 20.0 | 44.4 | 35.6
| CHD | 19.0 | 45.7 | 35.2
| GIH | 13.5 | 46.9 | 39.6
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 1.4 | 34.7 | 63.9
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{Venter SNP
|rsid=1130496
|allele=T
|frequency=
|uid=1103652756970
|type=homozygous_SNP
|hugo=PTPRN2
|ensembl gene=ENSG00000155093
|ensembl transcript=ENST00000331938
|sift=TOLERATED
|disease=Autoantigen in insulin-dependent diabetes mellitus (IDDM).
}}

{{ neighbor
| rsid = 1130495
| distance = 16
}}

{{PMID Auto
|PMID=19456320
|Title=A genome-wide association study of autism reveals a common novel risk locus at 5p14.1.
|OA=1
}}

{{GET Evidence
|gene=PTPRN2
|aa_change=Arg213His
|aa_change_short=R213H
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1130496
|overall_frequency_n=3687
|overall_frequency_d=10754
|overall_frequency=0.342849
|n_genomes=32
|n_genomes_annotated=0
|n_haplomes=40
|n_articles=0
|n_articles_annotated=0
|pph2_score=0.802
|nblosum100=1
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}