List of variants in gene POLD1 reported as benign by Department of Pathology and Laboratory Medicine, Sinai Health System

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_002691.4(POLD1):c.2244T>C (p.Ser748=)	rs1274607	0.10634
NM_002691.4(POLD1):c.1548C>T (p.Ala516=)	rs2230247	0.04514
NM_002691.4(POLD1):c.1539G>A (p.Leu513=)	rs2230246	0.04513
NM_002691.4(POLD1):c.1860G>A (p.Thr620=)	rs1726790	0.03590
NM_002691.4(POLD1):c.971-12C>T	rs1673044	0.03582
NM_002691.4(POLD1):c.234C>G (p.Arg78=)	rs2228665	0.03571
NM_002691.4(POLD1):c.518G>A (p.Ser173Asn)	rs1726803	0.03166
NM_002691.4(POLD1):c.1173C>T (p.Asp391=)	rs2230244	0.02764
NM_002691.4(POLD1):c.2154+13_2154+14insA	rs3218767	0.02057
NM_002691.4(POLD1):c.1713C>T (p.Pro571=)	rs2230248	0.01698
NM_002691.4(POLD1):c.2862G>C (p.Thr954=)	rs3219440	0.01109
NM_002691.4(POLD1):c.849G>T (p.Gln283His)	rs113282414	0.01085
NM_002691.4(POLD1):c.2275G>A (p.Val759Ile)	rs145473716	0.00110
NM_002691.4(POLD1):c.33C>T (p.Pro11=)	rs3218768	0.00109
NM_002691.4(POLD1):c.2628C>T (p.Ile876=)	rs75874199	0.00088
NM_002691.4(POLD1):c.1932C>G (p.Asp644Glu)	rs80214209	0.00041
NM_002691.4(POLD1):c.1791C>T (p.Pro597=)	rs138293440	0.00002

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