List of variants in gene combination POLG, POLGARF reported as benign for Inborn genetic diseases

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_002693.3(POLG):c.128A>G (p.Gln43Arg)	rs28567406	0.01433
NM_002693.3(POLG):c.126GCA[10] (p.Gln55del)	rs41550117
NM_002693.3(POLG):c.126GCA[12] (p.Gln55dup)	rs41550117
NM_002693.3(POLG):c.126GCA[13] (p.Gln54_Gln55dup)	rs41550117
NM_002693.3(POLG):c.126GCA[14] (p.Gln53_Gln55dup)	rs41550117

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