{{Rsnum
|rsid=2067051
|Gene=H19
|Chromosome=11
|position=1996938
|Orientation=minus
|GMAF=0.3448
|Gene_s=H19,MIR675
|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 | 31.0 | 41.6 | 27.4
| HCB | 7.3 | 38.7 | 54.0
| JPT | 10.6 | 39.8 | 49.6
| YRI | 0.0 | 6.1 | 93.9
| ASW | 1.8 | 26.3 | 71.9
| CHB | 7.3 | 38.7 | 54.0
| CHD | 6.4 | 51.4 | 42.2
| GIH | 6.9 | 45.5 | 47.5
| LWK | 0.9 | 9.1 | 90.0
| MEX | 17.2 | 41.4 | 41.4
| MKK | 3.8 | 28.2 | 67.9
| TSI | 22.5 | 56.9 | 20.6
| HapMapRevision=28
}}{{PMID Auto
|PMID=20639793
|Title=Association of birth weight with polymorphisms in the IGF2, H19, and IGF2R genes
|OA=1
}}

{{PMID|15885138|OA=1
}} Common polymorphism in H19 associated with birthweight and cord blood IGF-II levels in humans.

{{PMID|16839189|OA=1
}} Human imprinted chromosomal regions are historical hot-spots of recombination.

{{GET Evidence
|gene=H19
|aa_change=Val94Ile
|aa_change_short=V94I
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2067051
|overall_frequency_n=39
|overall_frequency_d=108
|overall_frequency=0.361111
|n_genomes=21
|n_genomes_annotated=0
|n_haplomes=29
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|genetests_testable=Y
|genetests_reviewed=Y
|nblosum100=-4
|autoscore=2
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}