List of variants in gene combination PDZD9, UQCRC2 reported as uncertain significance by GeneDx

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_003366.4(UQCRC2):c.1280C>T (p.Ala427Val)	rs145809522	0.00053
NM_003366.4(UQCRC2):c.416A>G (p.Asn139Ser)	rs529456792	0.00006
NM_003366.4(UQCRC2):c.291C>G (p.Phe97Leu)
NM_003366.4(UQCRC2):c.514C>T (p.His172Tyr)

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