Variant (rsID / SNP)

rs35776264

rs35776264 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYO7A. Location: chromosome 11, position 76,926,301. Clinical significance in the table: Likely benign.

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Reference-table entries

MYO7ALikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 11:76926301
Cytoband: 11q13.5
HGVS: NM_000260.3(MYO7A):c.*560C>T

Associated conditions / phenotypes

Nonsyndromic Hearing Loss, Dominant|Nonsyndromic Hearing Loss, Recessive|Retinitis pigmentosa-deafness syndrome

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.