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Variant (rsID / SNP)

rs368662693

POLE

rs368662693 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to POLE. Location: chromosome 12, position 133,209,251. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

POLEConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
12:133209251
Cytoband
12q24.33
HGVS
NM_006231.4(POLE):c.6135C>T (p.Pro2045=)
Allele change
Synonymous_P2045P

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.