List of variants in gene POLG reported as uncertain significance by ClinGen Mitochondrial Disease Nuclear and Mitochondrial Variant Curation Expert Panel, ClinGen

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_002693.3(POLG):c.3561G>C (p.Arg1187=)	rs62640037	0.00787
NM_002693.3(POLG):c.3294T>C (p.Asn1098=)	rs374224714	0.00011
NM_002693.3(POLG):c.3405C>T (p.Asp1135=)	rs2307445	0.00006
NM_002693.3(POLG):c.3451C>T (p.Leu1151=)	rs769193603	0.00004
NM_002693.3(POLG):c.3239G>C (p.Ser1080Thr)	rs779956099	0.00003
NM_002693.3(POLG):c.3483-14T>C	rs587781119

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