List of variants in gene POLD1 reported as likely benign by Fulgent Genetics, Fulgent Genetics

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: 10

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HGVS	dbSNP	gnomAD frequency
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.783C>T (p.Val261=)	rs34269084	0.00296
NM_002691.4(POLD1):c.778A>G (p.Ile260Val)	rs8105725	0.00295
NM_002691.4(POLD1):c.433G>A (p.Ala145Thr)	rs137953986	0.00253
NM_002691.4(POLD1):c.56G>A (p.Arg19His)	rs3218773	0.00197
NM_002691.4(POLD1):c.1785C>T (p.Asp595=)	rs769563176	0.00011
NM_002691.4(POLD1):c.1681C>A (p.Arg561=)	rs368738479	0.00001
NM_002691.4(POLD1):c.933C>T (p.Arg311=)	rs749278926	0.00001
NM_002691.4(POLD1):c.324G>T (p.Ala108=)	rs20582

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