{{Rsnum
|rsid=577948
|Gene=MIR100HG
|Chromosome=11
|position=122159482
|Orientation=plus
|GMAF=0.3632
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=MIR100HG
}}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
}}

{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 38.1 | 49.6 | 12.4
| HCB | 27.7 | 52.6 | 19.7
| JPT | 19.6 | 47.3 | 33.0
| YRI | 76.7 | 22.6 | 0.7
| ASW | 68.4 | 29.8 | 1.8
| CHB | 27.7 | 52.6 | 19.7
| CHD | 16.5 | 52.3 | 31.2
| GIH | 42.6 | 42.6 | 14.9
| LWK | 64.2 | 29.4 | 6.4
| MEX | 29.3 | 58.6 | 12.1
| MKK | 35.9 | 56.4 | 7.7
| TSI | 48.0 | 45.1 | 6.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19779542
|Trait=Myopia (pathological)
|Title=A genome-wide association analysis identified a novel susceptible locus for pathological myopia at 11q24.1
|RiskAllele=G
|Pval=2E-7
|OR=1.37
|ORtxt=[1.21-1.54]
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs577948
|overall_frequency_n=49
|overall_frequency_d=128
|overall_frequency=0.382812
|n_genomes=34
|n_genomes_annotated=0
|n_haplomes=40
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

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