List of variants in gene POLD1 reported as uncertain significance 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: 17

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HGVS	dbSNP	gnomAD frequency
NM_002691.4(POLD1):c.80A>T (p.Asp27Val)	rs150066950	0.00159
NM_002691.4(POLD1):c.1061C>T (p.Ala354Val)	rs140990974	0.00051
NM_002691.4(POLD1):c.2052G>C (p.Gln684His)	rs144143245	0.00045
NM_002691.4(POLD1):c.961G>A (p.Gly321Ser)	rs41554817	0.00029
NM_002691.4(POLD1):c.1795G>A (p.Ala599Thr)	rs149569984	0.00027
NM_002691.4(POLD1):c.2185G>A (p.Glu729Lys)	rs200931999	0.00016
NM_002691.4(POLD1):c.1562G>A (p.Arg521Gln)	rs143076166	0.00006
NM_002691.4(POLD1):c.2326C>T (p.Arg776Trp)	rs780138978	0.00006
NM_002691.4(POLD1):c.1322C>T (p.Thr441Met)	rs376711125	0.00005
NM_002691.4(POLD1):c.481A>T (p.Met161Leu)	rs763969133	0.00002
NM_002691.4(POLD1):c.1869G>T (p.Arg623=)	rs748380365	0.00001
NM_002691.4(POLD1):c.2953C>T (p.Arg985Trp)	rs780926432	0.00001
NM_002691.4(POLD1):c.327G>C (p.Gln109His)	rs750260438	0.00001
NM_002691.4(POLD1):c.429C>T (p.Gly143=)	rs372244044	0.00001
NM_002691.4(POLD1):c.1716G>T (p.Val572=)	rs1568628387
NM_002691.4(POLD1):c.208G>T (p.Val70Phe)	rs147911699
NM_002691.4(POLD1):c.2468G>T (p.Arg823Leu)	rs771734704

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