Variant (rsID / SNP)
rs58966182
rs58966182 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ODAD1. Location: chromosome 19, position 48,821,738. Clinical significance in the table: Benign.
Reference-table entries
ODAD1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 19:48821738
- Cytoband
- 19q13.33
- HGVS
- NM_001364171.2(ODAD1):c.266G>C (p.Arg89Pro)
- Allele change
- Missense_R89P
Associated conditions / phenotypes
Primary ciliary dyskinesia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.