Variant (rsID / SNP)

rs183256997

rs183256997 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYO15A. Location: chromosome 17, position 18,040,009. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

MYO15AConflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 17:18040009
Cytoband: 17p11.2
HGVS: NM_016239.4(MYO15A):c.4779+9G>A
Allele change: Silent

Associated conditions / phenotypes

Autosomal recessive nonsyndromic hearing loss 3

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.