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Variant (rsID / SNP)

rs202220778

POLE

rs202220778 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to POLE. Location: chromosome 12, position 133,263,886. 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
12:133263886
Cytoband
12q24.33
HGVS
NM_006231.4(POLE):c.16G>C (p.Gly6Arg)
Allele change
Missense_G6R

Associated conditions / phenotypes

Colorectal cancer|Colorectal cancer, susceptibility to, 12|Hereditary cancer-predisposing syndrome|Carcinoma of colon

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.