List of variants in gene NDUFA4 reported as benign 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_002489.4(NDUFA4):c.42+247T>C	rs1616965	0.67644
NM_002489.4(NDUFA4):c.190-43G>A	rs7789764	0.65599
NM_002489.4(NDUFA4):c.43-266T>A	rs2286978	0.33340
NM_002489.4(NDUFA4):c.189+87C>T	rs17163788	0.07061
NM_002489.4(NDUFA4):c.131+161T>C	rs10272132	0.05297
NM_002489.3(NDUFA4):c.-253T>C	rs112961586	0.03953
NM_002489.4(NDUFA4):c.42+207G>A	rs73061490	0.02588
NM_002489.4(NDUFA4):c.-13C>T	rs17163797	0.01406
NC_000007.14:g.10940291C>A	rs6961269
NM_002489.4(NDUFA4):c.43-120A>T	rs73678333

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