Variant (rsID / SNP)

rs375346333

rs375346333 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYO3A. Location: chromosome 10, position 26,454,985. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

MYO3AConflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 10:26454985
Cytoband: 10p12.1
HGVS: NM_017433.5(MYO3A):c.3000-11T>C
Allele change: Silent

Associated conditions / phenotypes

Autosomal recessive nonsyndromic hearing loss 30

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.