Variant (rsID / SNP)

rs28358569

rs28358569 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MT-RNR1. Clinical significance in the table: drug response.

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Reference-table entries

MT-RNR1Drug response

Clinical significance (as recorded): drug response
Variant type: single nucleotide variant
Cytoband: -
HGVS: NC_012920.1:m.827A>G
Allele change: Silent

Associated conditions / phenotypes

Mitochondrial non-syndromic sensorineural hearing loss|Aminoglycoside-induced deafness|Gentamicin response

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.