Variant (rsID / SNP)

rs56022846

rs56022846 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to POLD1. Location: chromosome 19, position 50,906,291. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

POLD1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 19:50906291
Cytoband: 19q13.33
HGVS: NM_002691.4(POLD1):c.971-19G>A
Allele change: Silent

Associated conditions / phenotypes

Colorectal cancer, susceptibility to, 10

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.