{{Rsnum
|rsid=1003484
|Gene=IGF2
|Chromosome=11
|position=2146388
|Orientation=plus
|ReferenceAllele=A
|MissenseAllele=G
|GMAF=0.3636
|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 | 0.0 | 0.0 | 0.0
| HCB | 0.0 | 0.0 | 0.0
| JPT | 0.0 | 0.0 | 0.0
| YRI | 9.5 | 54.0 | 36.5
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 0.0 | 0.0
| 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
}}

{{Venter SNP
|rsid=1003484
|allele=G
|frequency=
|uid=1103649586769
|type=homozygous_SNP
|hugo=IGF2AS
|ensembl gene=ENSG00000099869
|ensembl transcript=ENST00000381361
|sift=
|disease=Overexpressed in Wilms' tumor samples.
}}

{{ neighbor
| rsid = 1003483
| distance = 75
}}

{{GET Evidence
|gene=IGF2AS
|aa_change=Thr150Ala
|aa_change_short=T150A
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1003484
|overall_frequency_n=6886
|overall_frequency_d=9980
|overall_frequency=0.68998
|n_genomes=46
|n_genomes_annotated=0
|n_haplomes=68
|n_articles=0
|n_articles_annotated=0
|pph2_score=0.264
|nblosum100=1
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}