Variant (rsID / SNP)

rs34615182

rs34615182 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYO3A. Location: chromosome 10, position 26,465,671. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

MYO3ABenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 10:26465671
Cytoband: 10p12.1
HGVS: NM_017433.5(MYO3A):c.4335A>G (p.Lys1445=)
Allele change: Synonymous_K1445K

Associated conditions / phenotypes

Autosomal recessive nonsyndromic hearing loss 30

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.