{{Rsnum
|rsid=9589207
|Gene=MIR92A1
|Chromosome=13
|position=91351335
|Orientation=plus
|GMAF=0.02112
|Gene_s=MIR17HG,MIR92A1
|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 | 1.8 | 98.2
| HCB | 0.0 | 0.0 | 100.0
| JPT | 0.0 | 0.0 | 100.0
| YRI | 1.4 | 14.6 | 84.0
| ASW | 0.0 | 10.5 | 89.5
| CHB | 0.0 | 0.0 | 100.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.9 | 19.4 | 79.6
| MEX | 0.0 | 1.8 | 98.2
| MKK | 1.3 | 16.0 | 82.7
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}
{{snp near feature
| rsid = 9589207
| type = microRNA
| ACC=MI0000093
| ID=hsa-mir-92a-1
| offset=17
}}

{{PMID Auto
|PMID=18941528
|Title=Identification of a novel risk locus for multiple sclerosis at 13q31.3 by a pooled genome-wide scan of 500,000 single nucleotide polymorphisms.
|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
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}