Variant (rsID / SNP)
rs76879328
rs76879328 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CFTR. Location: chromosome 7, position 117,180,359. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
CFTRConflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 7:117180359
- Cytoband
- 7q31.2
- HGVS
- NM_000492.4(CFTR):c.1075C>A (p.Gln359Lys)
- Allele change
- Missense_Q359K
Associated conditions / phenotypes
Hereditary pancreatitis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.