"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "POLD1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2683517	NM_002691.4(POLD1):c.203-3C>G	POLD1	Single nucleotide variant (intron variant)	Colorectal cancer, susceptibility to, 10 +1 more	GUncertain significance
Select item 225288	NM_002691.4(POLD1):c.208G>T (p.Val70Phe)	POLD1 (V70F)	Single nucleotide variant (missense variant +1 more)	Colorectal cancer, susceptibility to, 10 +5 more	GConflicting classifications of pathogenicity
Select item 221136	NM_002691.4(POLD1):c.961G>A (p.Gly321Ser)	POLD1 (G321S)	Single nucleotide variant (missense variant +1 more)	not provided +5 more	GConflicting classifications of pathogenicity
Select item 484390	NM_002691.4(POLD1):c.1148C>T (p.Thr383Ile)	POLD1 (T383I)	Single nucleotide variant (missense variant +1 more)	Colorectal cancer, susceptibility to, 10 +3 more	GConflicting classifications of pathogenicity
Select item 408020	NM_002691.4(POLD1):c.1937T>A (p.Phe646Tyr)	POLD1 (F646Y +1 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 537048	NM_002691.4(POLD1):c.3121-9C>A	POLD1	Single nucleotide variant (intron variant)	not provided +1 more	GUncertain significance

ClinVar