{{Rsnum
|rsid=11066301
|Gene=PTPN11
|Chromosome=12
|position=112433568
|Orientation=plus
|GMAF=0.2006
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=PTPN11
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 41.6 | 45.1 | 13.3
| HCB | 99.3 | 0.7 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 98.4 | 1.6 | 0.0
| ASW | 84.2 | 14.0 | 1.8
| CHB | 99.3 | 0.7 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 78.2 | 19.8 | 2.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 65.5 | 31.0 | 3.4
| MKK | 0.0 | 0.0 | 0.0
| TSI | 22.8 | 53.5 | 23.8
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=19820697
|Trait=Hematological parameters
|Title=A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium
|RiskAllele=G
|Pval=8E-12
|OR=4.65
|ORtxt=[3.32-5.98] 10^9/l increase
|OA=1
}}

{{PMID Auto
|PMID=19862010
|Title=Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.
|OA=1
}}

{{PMID Auto
|PMID=21193429
|Title=Determinants of platelet count in humans.
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs11066301
|overall_frequency_n=25
|overall_frequency_d=128
|overall_frequency=0.195312
|n_genomes=20
|n_genomes_annotated=0
|n_haplomes=22
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

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