Variant (rsID / SNP)

rs111033389

rs111033389 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYO7A. Location: chromosome 11, position 76,874,035. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

MYO7ALikely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 11:76874035
Cytoband: 11q13.5
HGVS: NM_000260.4(MYO7A):c.1690+1G>A
Allele change: Silent

Associated conditions / phenotypes

Rare genetic deafness

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.