{{Rsnum
|rsid=8191754
|Gene=IGF2R
|Chromosome=6
|position=160027292
|Orientation=plus
|GMAF=0.1419
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=IGF2R
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 70.8 | 27.7 | 1.5
| HCB | 68.9 | 22.2 | 8.9
| JPT | 64.4 | 28.9 | 6.7
| YRI | 60.7 | 39.3 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 68.9 | 22.2 | 8.9
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=20639793
|Title=Association of birth weight with polymorphisms in the IGF2, H19, and IGF2R genes
|OA=1
}}

{{PMID|19435860|OA=1
}} IGF2R missense single-nucleotide polymorphisms and breast cancer risk: the multiethnic cohort study.

{{GET Evidence
|gene=IGF2R
|aa_change=Leu252Val
|aa_change_short=L252V
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs8191754
|overall_frequency_n=1453
|overall_frequency_d=10756
|overall_frequency=0.135087
|n_genomes=17
|n_genomes_annotated=0
|n_haplomes=20
|n_articles=0
|n_articles_annotated=0
|pph2_score=0.787
|nblosum100=0
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}