{{Rsnum
|rsid=1566667
|Chromosome=12
|position=130127245
|Orientation=plus
|GMAF=0.2319
|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 | 1.8 | 18.6 | 79.6
| HCB | 6.7 | 42.5 | 50.7
| JPT | 3.5 | 33.6 | 62.8
| YRI | 12.3 | 51.4 | 36.3
| ASW | 8.9 | 51.8 | 39.3
| CHB | 6.7 | 42.5 | 50.7
| CHD | 7.4 | 44.4 | 48.1
| GIH | 11.0 | 44.0 | 45.0
| LWK | 21.1 | 48.6 | 30.3
| MEX | 3.4 | 17.2 | 79.3
| MKK | 14.6 | 41.1 | 44.4
| TSI | 2.0 | 19.6 | 78.4
| HapMapRevision=28
}}

This SNP, rs1566667, was mentioned as one of the SNPs defining a haplotype used during a search for a deafness-associated gene on chromosome 12. However, rs1566667 itself has no reported associations with deafness (or any other condition).

{{PMID Auto
|PMID=16195816
|Title=Refinement of the DFNA41 locus and candidate genes analysis.
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}