{{Rsnum
|rsid=2289030
|Gene=KRT19P2
|Chromosome=12
|position=94834510
|Orientation=minus
|GMAF=0.118
|Gene_s=KRT19P2,MIR492
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 81.5 | 18.5 | 0.0
| HCB | 59.1 | 34.1 | 6.8
| JPT | 48.8 | 41.5 | 9.8
| YRI | 100.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 59.1 | 34.1 | 6.8
| 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=20044760
|Title=Prognostic impact of microRNA-related gene polymorphisms on survival of patients with colorectal cancer
}}

{{PMID Auto
|PMID=19047128
|Title=Single nucleotide polymorphisms of microRNA machinery genes modify the risk of renal cell carcinoma.
|OA=1
}}

{{PMID Auto
|PMID=19138993
|Title=Genetic variations in microRNA-related genes are novel susceptibility loci for esophageal cancer risk.
|OA=1
}}

{{PMID Auto
|PMID=19232555
|Title=Signatures of purifying and local positive selection in human miRNAs.
|OA=1
}}

{{PMID Auto
|PMID=19458495
|Title=Comprehensive analysis of the impact of SNPs and CNVs on human microRNAs and their regulatory genes.
|OA=1
}}

{{PMID Auto
|PMID=22818121
|Title=The prognostic impact of microRNA sequence polymorphisms on the recurrence of patients with completely resected non-small cell lung cancer
}}

{{on chip | Illumina Human 1M}}