Variant (rsID / SNP)

rs61732929

rs61732929 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to POLE. Location: chromosome 12, position 133,253,974. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

POLEBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 12:133253974
Cytoband: 12q24.33
HGVS: NM_006231.4(POLE):c.776G>A (p.Arg259His)
Allele change: Missense_R259H

Associated conditions / phenotypes

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

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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