Variant (rsID / SNP)
rs770466844
rs770466844 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to POLE. Location: chromosome 12, position 133,218,443. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
POLEConflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:133218443
- Cytoband
- 12q24.33
- HGVS
- NM_006231.4(POLE):c.5174-6G>C
- Allele change
- Silent
Associated conditions / phenotypes
Colorectal cancer, susceptibility to, 12|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.