Gene entry
MYO6
myosin VI
- Chromosome
- 6
- Cytoband
- 6q14.1
- Variants (rsID)
- 29
MYO6 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 6 (region 6q14.1). Its official name is “myosin VI”. The reference table lists 29 variants (rsID) for this gene.
Clinically classified variants
10 reference-table entries with clinical significance.
- rs1341567Benignsingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 22|Autosomal recessive nonsyndromic hearing loss 37
- rs145564837Benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 37|Autosomal dominant nonsyndromic hearing loss 22|Nonsyndromic genetic hearing loss
- rs121912559Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 37|Autosomal dominant nonsyndromic hearing loss 22
- rs139664153Conflicting interpretationssingle nucleotide variant
- rs373199401Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 37|Autosomal dominant nonsyndromic hearing loss 22
- rs41269323Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 37|Autosomal dominant nonsyndromic hearing loss 22
- rs565770950Conflicting interpretationssingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 22|Autosomal recessive nonsyndromic hearing loss 37
- rs121912560Likely pathogenicsingle nucleotide variantSensorineural deafness with hypertrophic cardiomyopathy|Rare genetic deafness
- rs727504567Likely pathogenicsingle nucleotide variantNonsyndromic genetic hearing loss|Rare genetic deafness|Autosomal dominant nonsyndromic hearing loss 22
- rs189411232Uncertain significancesingle nucleotide variant
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.