List of variants in gene combination FANCI, POLG reported as benign by Breakthrough Genomics, Breakthrough Genomics

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_002693.3(POLG):c.3643+257T>G	rs1061316	0.48343
NM_002693.3(POLG):c.3428A>G (p.Glu1143Gly)	rs2307441	0.02704
NC_000015.10:g.89317316C>A	rs3176236
NM_002693.3(POLG):c.3643+226C>G	rs1860022

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