{{Rsnum
|rsid=107822
|Gene=RING1
|Chromosome=6
|position=33207798
|Orientation=minus
|GMAF=0.3623
|Gene_s=MIR219A1,RING1
|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 | 5.3 | 42.5 | 52.2
| HCB | 36.3 | 41.5 | 22.2
| JPT | 49.6 | 36.3 | 14.2
| YRI | 12.9 | 40.8 | 46.3
| ASW | 12.5 | 33.9 | 53.6
| CHB | 36.3 | 41.5 | 22.2
| CHD | 44.0 | 43.1 | 12.8
| GIH | 10.9 | 51.5 | 37.6
| LWK | 23.6 | 42.7 | 33.6
| MEX | 6.9 | 27.6 | 65.5
| MKK | 9.6 | 53.8 | 36.5
| TSI | 7.8 | 38.2 | 53.9
| HapMapRevision=28
}}{{PMID Auto
|PMID=23029284
|Title=Comprehensive exploration of the effects of miRNA SNPs on monocyte gene expression
|OA=1
}}

{{PMID Auto
|PMID=23508906
|Title=Association of polymorphism in MicroRNA 219-1 with clearance of hepatitis B virus infection
}}

{{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
}}

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