List of variants in gene POLD1 reported as benign by Counsyl

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: 6

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HGVS	dbSNP	gnomAD frequency
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.88C>T (p.Arg30Trp)	rs3218772	0.00706
NM_002691.4(POLD1):c.2546G>A (p.Arg849His)	rs3218775	0.00670
NM_002691.4(POLD1):c.56G>A (p.Arg19His)	rs3218773	0.00197
NM_002691.4(POLD1):c.1776-83del	rs751745933

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