Variant (rsID / SNP)
rs397508669
rs397508669 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CFTR. Location: chromosome 7, position 117,304,864. Clinical significance in the table: Pathogenic.
Reference-table entries
CFTRPathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- Duplication
- Chromosome / position
- 7:117304864
- Cytoband
- 7q31.2
- HGVS
- NM_000492.4(CFTR):c.4086dup (p.Lys1363Ter)
Associated conditions / phenotypes
Cystic fibrosis|CFTR-related disorders
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.