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Variant (rsID / SNP)

rs184866544

MYO7A

rs184866544 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYO7A. Location: chromosome 11, position 76,868,392. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

MYO7AConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
11:76868392
Cytoband
11q13.5
HGVS
NM_000260.4(MYO7A):c.803A>G (p.Lys268Arg)
Allele change
Missense_K268R

Associated conditions / phenotypes

Autosomal dominant nonsyndromic hearing loss 11|Usher syndrome type 1|Autosomal recessive nonsyndromic hearing loss 2

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.