{{Rsnum
|rsid=1027557
|Chromosome=12
|position=130120384
|Orientation=plus
|GMAF=0.2893
|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 | 55.8 | 40.7 | 3.5
| HCB | 48.5 | 39.0 | 12.5
| JPT | 43.4 | 47.8 | 8.8
| YRI | 31.5 | 52.7 | 15.8
| ASW | 49.1 | 35.1 | 15.8
| CHB | 48.5 | 39.0 | 12.5
| CHD | 51.4 | 45.0 | 3.7
| GIH | 57.4 | 34.7 | 7.9
| LWK | 30.9 | 54.5 | 14.5
| MEX | 53.4 | 39.7 | 6.9
| MKK | 25.6 | 48.7 | 25.6
| TSI | 60.4 | 36.6 | 3.0
| HapMapRevision=28
}}
This SNP, [[rs1027557]], was mentioned as one of the SNPs defining a haplotype used during a search for a deafness-associated gene on chromosome 12. However, [[rs1027557]] 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 | HumanOmni1Quad}}