Variant (rsID / SNP)
rs2728121
rs2728121 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PKD2. Location: chromosome 4, position 88,997,102. Clinical significance in the table: Benign.
Reference-table entries
PKD2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 4:88997102
- Cytoband
- 4q22.1
- HGVS
- NM_000297.4(PKD2):c.*256C>T
- Allele change
- Silent
Associated conditions / phenotypes
Polycystic kidney disease 2
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.