Variant (rsID / SNP)
rs111033201
rs111033201 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYO7A. Location: chromosome 11, position 76,885,871. Clinical significance in the table: Pathogenic/Likely pathogenic.
Reference-table entries
MYO7APathogenic
- Clinical significance (as recorded)
- Pathogenic/Likely pathogenic
- Variant type
- single nucleotide variant
- Chromosome / position
- 11:76885871
- Cytoband
- 11q13.5
- HGVS
- NM_000260.4(MYO7A):c.2005C>T (p.Arg669Ter)
- Allele change
- Nonsense_R669X
Associated conditions / phenotypes
Usher syndrome type 1|Autosomal recessive nonsyndromic hearing loss 2|Usher syndrome|Autosomal dominant nonsyndromic hearing loss 11|Autosomal recessive nonsyndromic hearing loss 2|Usher syndrome type 1|Rare genetic deafness|Usher syndrome type 1B
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.