{{Rsnum
|rsid=9854612
|Chromosome=3
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=TMED10P2
|position=128538371
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 8.0 | 36.3 | 55.8
| HCB | 17.5 | 49.6 | 32.8
| JPT | 23.0 | 43.4 | 33.6
| YRI | 38.1 | 53.7 | 8.2
| ASW | 28.1 | 59.6 | 12.3
| CHB | 17.5 | 49.6 | 32.8
| CHD | 17.4 | 47.7 | 34.9
| GIH | 8.9 | 35.6 | 55.4
| LWK | 56.4 | 37.3 | 6.4
| MEX | 10.3 | 39.7 | 50.0
| MKK | 44.5 | 40.6 | 14.8
| TSI | 16.7 | 42.2 | 41.2
| HapMapRevision=28
}}Strongest association with combined capacities for music perception (pitch, duration, sound patterns) found in study of 767 Finnish individuals belonging in 76 families {{PMID|24614497}}, involved in [[musical aptitude]]. [[PPLD|Posterior probability of LD]] 98%.

This region is located a few dozen kilobases upstream of the GATA binding protein 2 [[GATA2]] gene. [[GATA2]] regulates the development of cochlear hair cells and the inferior colliculus (IC), which are important in tonotopic mapping. [[SNP]] is surrounded by known regulatory regions, and may itself be in one.

[http://www.nature.com/mp/journal/vaop/ncurrent/abs/mp20148a.html A genome-wide linkage and association study of musical aptitude identifies loci containing genes related to inner ear development and neurocognitive functions]

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}