Variant (rsID / SNP)
rs72478580
rs72478580 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRLR. Location: chromosome 5, position 35,072,712. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
PRLRConflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 5:35072712
- Cytoband
- 5p13.2
- HGVS
- NM_000949.7(PRLR):c.508A>C (p.Ile170Leu)
- Allele change
- Missense_I170L
Associated conditions / phenotypes
Multiple fibroadenoma of the breast
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.