Variant (rsID / SNP)

rs199474824

rs199474824 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MT-RNR2. Clinical significance in the table: Pathogenic.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

MT-RNR2Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Cytoband: -
HGVS: m.2939C>A
Allele change: Silent

Associated conditions / phenotypes

Chloramphenicol resistance

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.