Variant (rsID / SNP)

rs111033426

rs111033426 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYO7A. Location: chromosome 11, position 76,853,754. 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: 11:76853754
Cytoband: 11q13.5
HGVS: NM_000260.4(MYO7A):c.19-1G>A
Allele change: Silent

Associated conditions / phenotypes

Rare genetic deafness|Usher syndrome type 1|Autosomal recessive nonsyndromic hearing loss 2

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.