{{Rsnum
|rsid=854777
|Gene=MYO15A
|Chromosome=17
|position=18143584
|Orientation=minus
|ReferenceAllele=T
|MissenseAllele=C
|GMAF=0.2466
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=MYO15A
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 2.7 | 41.4 | 55.9
| HCB | 12.6 | 53.3 | 34.1
| JPT | 12.4 | 54.0 | 33.6
| YRI | 0.7 | 19.9 | 79.5
| ASW | 3.5 | 10.5 | 86.0
| CHB | 12.6 | 53.3 | 34.1
| CHD | 14.7 | 49.5 | 35.8
| GIH | 24.2 | 50.5 | 25.3
| LWK | 0.9 | 20.0 | 79.1
| MEX | 8.9 | 37.5 | 53.6
| MKK | 1.9 | 15.4 | 82.7
| TSI | 8.8 | 46.1 | 45.1
| HapMapRevision=28
}}{{Venter SNP
|rsid=854777
|allele=C
|frequency=0.767
|uid=1103645293753
|type=homozygous_SNP
|hugo=MYO15A
|ensembl gene=ENSG00000091536
|ensembl transcript=ENST00000205890
|sift=TOLERATED
|disease=Defects in MYO15A are the cause of autosomal recessive nonsyndromic deafness type 3 (DFNB3) (MIM:600316).
}}

{{PMID Auto
|PMID=18776599
|Title=Susceptibility genes for gentamicin-induced vestibular dysfunction.
|OA=1
}}

{{GET Evidence
|gene=MYO15A
|aa_change=Cys1975Arg
|aa_change_short=C1975R
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs854777
|overall_frequency_n=93
|overall_frequency_d=128
|overall_frequency=0.726562
|n_genomes=48
|n_genomes_annotated=0
|n_haplomes=81
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|genetests_testable=Y
|nblosum100=8
|autoscore=1
|webscore=N
}}

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