{{Rsnum
|rsid=2251375
|Gene=H19
|Chromosome=11
|position=1998266
|Orientation=plus
|GMAF=0.4408
|Gene_s=H19,MIR675
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 9.2 | 40.0 | 50.8
| HCB | 26.7 | 35.6 | 37.8
| JPT | 25.0 | 45.5 | 29.5
| YRI | 60.3 | 30.2 | 9.5
| ASW | 0.0 | 0.0 | 0.0
| CHB | 26.7 | 35.6 | 37.8
| 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 Auto
|PMID=16839189
|Title=Human imprinted chromosomal regions are historical hot-spots of recombination.
|OA=1
}}

{{PMID Auto
|PMID=19543528
|Title=Association between common germline genetic variation in 94 candidate genes or regions and risks of invasive epithelial ovarian cancer.
|OA=1
}}