Variant (rsID / SNP)

rs1341567

rs1341567 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYO6. Location: chromosome 6, position 76,628,176. 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: 6:76628176
Cytoband: 6q14.1
HGVS: NM_004999.4(MYO6):c.*3447A>C
Allele change: Silent

Associated conditions / phenotypes

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

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.