{{Rsnum
|rsid=712270
|Gene=MYO15A
|Chromosome=17
|position=18153853
|Orientation=plus
|ReferenceAllele=A
|MissenseAllele=T
|GMAF=0.2466
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene_s=MYO15A
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;T)
| geno3=(T;T)
| CEU | 19.0 | 46.0 | 34.9
| HCB | 0.0 | 15.6 | 84.4
| JPT | 0.0 | 18.2 | 81.8
| YRI | 3.2 | 30.2 | 66.7
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 15.6 | 84.4
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{Venter SNP
|rsid=712270
|allele=T
|frequency=0.462
|uid=1103645293779
|type=homozygous_SNP
|hugo=MYO15A
|ensembl gene=ENSG00000091536
|ensembl transcript=ENST00000205890
|sift=
|disease=Defects in MYO15A are the cause of autosomal recessive nonsyndromic deafness type 3 (DFNB3) (MIM:600316).
}}

{{GET Evidence
|gene=MYO15A
|aa_change=Tyr2680Phe
|aa_change_short=Y2680F
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs712270
|overall_frequency_n=4
|overall_frequency_d=56
|overall_frequency=0.0714286
|n_genomes=2
|n_genomes_annotated=0
|n_haplomes=2
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|genetests_testable=Y
|nblosum100=-4
|autoscore=1
|webscore=N
}}

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