{{Rsnum
|rsid=1052030
|Gene=MYO7A
|Chromosome=11
|position=77142737
|Orientation=plus
|ReferenceAllele=T
|MissenseAllele=C
|GMAF=0.4853
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=MYO7A
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 13.4 | 33.0 | 53.6
| HCB | 26.1 | 44.0 | 29.9
| JPT | 23.2 | 54.5 | 22.3
| YRI | 74.6 | 23.2 | 2.1
| ASW | 49.1 | 47.4 | 3.5
| CHB | 26.1 | 44.0 | 29.9
| CHD | 26.6 | 52.3 | 21.1
| GIH | 19.8 | 52.5 | 27.7
| LWK | 63.2 | 34.9 | 1.9
| MEX | 15.8 | 40.4 | 43.9
| MKK | 0.0 | 0.0 | 0.0
| TSI | 14.7 | 49.0 | 36.3
| HapMapRevision=28
}}

{{Venter SNP
|rsid=1052030
|allele=C
|frequency=0.3
|uid=1103649728653
|type=heterozygous_SNP
|hugo=MYO7A
|ensembl gene=ENSG00000137474
|ensembl transcript=ENST00000358342
|sift=TOLERATED
|disease=Defects in MYO7A are the cause of autosomal dominant nonsyndromic sensorineural deafness 11 (DFNA11) (MIM:601317). DFNA11 is a form of nonsyndromic sensorineural deafness with onset after complete speech acquisition and subsequent gradual progression.
}}

{{ClinVar
|rsid=1052030
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=76853783
|CHROM=11
|GMAF=0.4858
|dbSNPBuildID=86
|SSR=0
|SAO=1
|VP=0x05016800000017051f100101
|GENEINFO=MYO7A:4647
|GENE_NAME=MYO7A
|GENE_ID=4647
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.76853783T>C
|CLNORIGIN=1
|CLNSIG=2
|Tags=PM;PMC;SLO;VLD;G5A;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;PH3;LSD
|CAF=0.5147; 0.4853
|CLNACC=RCV000036163.1
|CLNDBN=AllHighlyPenetrant
|CLNDSDB=MedGen
|CLNDSDBID=CN169374
|COMMON=1
|Disease=AllHighlyPenetrant
}}

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

{{GET Evidence
|gene=MYO7A
|aa_change=Leu16Ser
|aa_change_short=L16S
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1052030
|overall_frequency_n=4839
|overall_frequency_d=10298
|overall_frequency=0.469897
|n_genomes=40
|n_genomes_annotated=0
|n_haplomes=59
|n_articles=0
|n_articles_annotated=0
|qualityscore_in_silico=2
|qualitycomment_in_silico=Y
|gene_in_genetests=Y
|genetests_testable=Y
|genetests_reviewed=Y
|nblosum100=6
|autoscore=3
|n_web_uneval=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Affy500k}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}