Variant (rsID / SNP)
rs1057521166
rs1057521166 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to POLD1. Location: chromosome 19, position 50,919,789. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
POLD1Conflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 19:50919789
- Cytoband
- 19q13.33
- HGVS
- NM_002691.4(POLD1):c.2953+4C>T
- Allele change
- Silent
Associated conditions / phenotypes
Colorectal cancer, susceptibility to, 10|Hereditary cancer-predisposing syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.