{{Rsnum
|rsid=11218544
|Gene=MIR100HG
|Chromosome=11
|position=122168344
|Orientation=plus
|GMAF=0.2002
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=MIR100HG
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 3.5 | 32.7 | 63.7
| HCB | 16.1 | 48.9 | 35.0
| JPT | 14.2 | 37.2 | 48.7
| YRI | 0.0 | 12.2 | 87.8
| ASW | 0.0 | 21.1 | 78.9
| CHB | 16.1 | 48.9 | 35.0
| CHD | 10.1 | 50.5 | 39.4
| GIH | 5.0 | 45.5 | 49.5
| LWK | 0.0 | 10.9 | 89.1
| MEX | 0.0 | 19.0 | 81.0
| MKK | 0.6 | 18.6 | 80.8
| TSI | 3.9 | 39.2 | 56.9
| HapMapRevision=28
}}Despite two previous GWAS studies associating this SNP with high myopia in Japanese populations, no association was seen in a Chinese population studied.{{PMID|22194655|OA=1
}}

{{PMID|19779542|OA=1
}} A genome-wide association analysis identified a novel susceptible locus for pathological myopia at 11q24.1.

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