Variant (rsID / SNP)

rs375365167

rs375365167 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to POLD1. Location: chromosome 19, position 50,902,313. Clinical significance in the table: Uncertain significance.

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Reference-table entries

POLD1Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 19:50902313
Cytoband: 19q13.33
HGVS: NM_002691.4(POLD1):c.202+3A>G
Allele change: Silent

Associated conditions / phenotypes

Colorectal cancer, susceptibility to, 10|Hereditary cancer-predisposing syndrome

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.