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Variant (rsID / SNP)

rs145564837

MYO6

rs145564837 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYO6. Location: chromosome 6, position 76,558,195. Clinical significance in the table: Benign.

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Reference-table entries

MYO6Benign
Clinical significance (as recorded)
Benign
Variant type
single nucleotide variant
Chromosome / position
6:76558195
Cytoband
6q14.1
HGVS
NM_004999.4(MYO6):c.1025C>T (p.Ala342Val)
Allele change
Missense_A342V

Associated conditions / phenotypes

Autosomal recessive nonsyndromic hearing loss 37|Autosomal dominant nonsyndromic hearing loss 22|Nonsyndromic genetic hearing loss

Public references

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