{{Rsnum
|rsid=10770125
|Gene=INS-IGF2
|Chromosome=11
|position=2147784
|Orientation=plus
|GMAF=0.3848
|Gene_s=IGF2,INS-IGF2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 31.9 | 45.1 | 23.0
| HCB | 35.6 | 50.4 | 14.1
| JPT | 28.6 | 50.9 | 20.5
| YRI | 80.3 | 17.7 | 2.0
| ASW | 66.7 | 29.8 | 3.5
| CHB | 35.6 | 50.4 | 14.1
| CHD | 44.0 | 42.2 | 13.8
| GIH | 50.5 | 41.6 | 7.9
| LWK | 77.3 | 20.9 | 1.8
| MEX | 20.7 | 41.4 | 37.9
| MKK | 72.4 | 25.0 | 2.6
| TSI | 32.4 | 49.0 | 18.6
| HapMapRevision=28
}}{{PMID Auto
|PMID=21926269
|Title=Associations between paternally transmitted fetal IGF2 variants and maternal circulating glucose concentrations in pregnancy
|OA=1
}}

{{PMID Auto
|PMID=18769151
|Title=A sensitive functional assay reveals frequent loss of genomic imprinting in human placenta.
|OA=1
}}

{{GET Evidence
|gene=NM_001042376
|aa_change=Leu144Pro
|aa_change_short=L144P
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs10770125
|overall_frequency_n=2902
|overall_frequency_d=8400
|overall_frequency=0.345476
|n_genomes=32
|n_genomes_annotated=0
|n_haplomes=42
|n_articles=0
|n_articles_annotated=0
|nblosum100=7
|autoscore=0
|webscore=N
}}

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