ClinVar Miner

List of variants in gene combination FANCI, POLG reported 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
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_002693.3(POLG):c.3428A>G (p.Glu1143Gly)	rs2307441	0.02704
NM_002693.3(POLG):c.*100G>A	rs770839560	0.00012
NM_002693.3(POLG):c.*122G>A	rs886051517	0.00009
NM_002693.3(POLG):c.*420A>G	rs2055257867

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