Related gene-specific medical variations for Gene (Select 57804) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3308325	NM_021173.5(POLD4):c.29C>G (p.Ser10Cys)	LOC100130987, POLD4 (S10C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3308324	NM_021173.5(POLD4):c.308A>G (p.His103Arg)	LOC100130987, POLD4 (H103R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3216314	NM_021173.5(POLD4):c.197G>T (p.Arg66Leu)	LOC100130987, POLD4 (R66L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2642013	NM_021173.5(POLD4):c.174C>T (p.Tyr58=)	LOC100130987, POLD4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2381755	NM_021173.5(POLD4):c.166T>C (p.Trp56Arg)	LOC100130987, POLD4 (W56R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2350245	NM_021173.5(POLD4):c.241C>A (p.Pro81Thr)	LOC100130987, POLD4 (P81T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2320541	NM_021173.5(POLD4):c.35C>T (p.Pro12Leu)	LOC100130987, POLD4 (P12L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2310789	NM_021173.5(POLD4):c.55G>A (p.Gly19Arg)	LOC100130987, POLD4 (G19R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar