{{Rsnum
|rsid=7911488
|Gene=USMG5
|Chromosome=10
|position=105154089
|Orientation=plus
|GMAF=0.2668
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=131
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 44.2 | 43.4 | 12.4
| HCB | 48.1 | 41.5 | 10.4
| JPT | 41.1 | 43.8 | 15.2
| YRI | 93.9 | 6.1 | 0.0
| ASW | 87.5 | 12.5 | 0.0
| CHB | 48.1 | 41.5 | 10.4
| CHD | 43.0 | 47.7 | 9.3
| GIH | 15.8 | 53.5 | 30.7
| LWK | 90.9 | 8.2 | 0.9
| MEX | 51.7 | 41.4 | 6.9
| MKK | 80.0 | 20.0 | 0.0
| TSI | 32.4 | 49.0 | 18.6
| HapMapRevision=28
}}

{{snp near feature
| rsid = 7911488
| type = microRNA
| ACC=MI0006444
| ID=hsa-mir-1307
| offset=-5
}}

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

{{PMID|19680542|OA=1
}} Tissue effect on genetic control of transcript isoform variation.

{{PMID|20011102|OA=1
}} Fine-scale variation and genetic determinants of alternative splicing across individuals.

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