List of variants in gene POLD1 reported as likely benign by True Health Diagnostics

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: 29

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
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.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.1713C>T (p.Pro571=)	rs2230248	0.01698
NM_002691.4(POLD1):c.849G>T (p.Gln283His)	rs113282414	0.01085
NM_002691.4(POLD1):c.1761C>T (p.Ile587=)	rs3218755	0.00976
NM_002691.4(POLD1):c.88C>T (p.Arg30Trp)	rs3218772	0.00706
NM_002691.4(POLD1):c.783C>T (p.Val261=)	rs34269084	0.00296
NM_002691.4(POLD1):c.778A>G (p.Ile260Val)	rs8105725	0.00295
NM_002691.4(POLD1):c.1977C>T (p.Ile659=)	rs45605236	0.00290
NM_002691.4(POLD1):c.56G>A (p.Arg19His)	rs3218773	0.00197
NM_002691.4(POLD1):c.378C>T (p.Arg126=)	rs145324823	0.00188
NM_002691.4(POLD1):c.2967G>A (p.Thr989=)	rs3218752	0.00142
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.1620C>T (p.Gly540=)	rs140216790	0.00098
NM_002691.4(POLD1):c.2628C>T (p.Ile876=)	rs75874199	0.00088
NM_002691.4(POLD1):c.1138-8A>G	rs41544624	0.00056
NM_002691.4(POLD1):c.1665C>T (p.Val555=)	rs150238541	0.00053
NM_002691.4(POLD1):c.2103C>T (p.Tyr701=)	rs201483538	0.00046
NM_002691.4(POLD1):c.1182C>T (p.Thr394=)	rs377462923	0.00009
NM_002691.4(POLD1):c.1695C>T (p.His565=)	rs763347860	0.00002
NM_002691.4(POLD1):c.2136G>A (p.Pro712=)	rs765207547	0.00002
NM_002691.4(POLD1):c.2427C>T (p.Tyr809=)	rs775317882	0.00002
NM_002691.4(POLD1):c.324G>T (p.Ala108=)	rs20582
NM_002691.4(POLD1):c.463+8_463+9delinsTT	rs796285537

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.