Variant (rsID / SNP)

rs1006770

rs1006770 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYO15A. Location: chromosome 17, position 18,058,461. 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: 17:18058461
Cytoband: 17p11.2
HGVS: NM_016239.4(MYO15A):c.8262G>A (p.Thr2754=)
Allele change: Synonymous_T2754T

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.