Variant (rsID / SNP)
rs1877687
rs1877687 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAI2. Location: chromosome 17, position 72,270,442. Clinical significance in the table: Benign.
Reference-table entries
DNAI2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 17:72270442
- Cytoband
- 17q25.1
- HGVS
- NM_023036.6(DNAI2):c.-54A>G
- Allele change
- Silent
Associated conditions / phenotypes
Primary ciliary dyskinesia 9
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.