{{Rsnum
|rsid=180275
|Gene=GNGT1
|Chromosome=7
|position=93906158
|Orientation=minus
|GMAF=0.0932
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=GNGT1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 84.1 | 14.2 | 1.8
| HCB | 86.1 | 13.9 | 0.0
| JPT | 81.4 | 15.9 | 2.7
| YRI | 83.0 | 15.6 | 1.4
| ASW | 92.9 | 7.1 | 0.0
| CHB | 86.1 | 13.9 | 0.0
| CHD | 89.8 | 10.2 | 0.0
| GIH | 81.2 | 17.8 | 1.0
| LWK | 71.8 | 27.3 | 0.9
| MEX | 79.3 | 20.7 | 0.0
| MKK | 73.7 | 23.7 | 2.6
| TSI | 82.4 | 16.7 | 1.0
| HapMapRevision=28
}}
{{PMID|16280132}} rs180275(G) associated with increased risk of sudden [[deafness]] in Korean population. odds ratio (OR) for SD associated with the G vs. A allele was 2.58

{{PMID|18433792}} rs180275 G allele protective against an increase in BMI in Korean population.

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