List of variants reported as benign for mitochondrial complex V (ATP synthase) deficiency nuclear type 2 by Labcorp Genetics (formerly Invitae), Labcorp

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_017866.6(TMEM70):c.777C>G (p.Asp259Glu)	rs1053077	0.23539
NM_017866.6(TMEM70):c.748A>G (p.Thr250Ala)	rs1053079	0.23525
NM_017866.6(TMEM70):c.100G>C (p.Ala34Pro)	rs8075	0.17369
NM_017866.6(TMEM70):c.346C>G (p.Leu116Val)	rs61732273	0.02073
NM_017866.6(TMEM70):c.379A>G (p.Thr127Ala)	rs61734099	0.01433
NM_017866.6(TMEM70):c.580G>A (p.Val194Met)	rs77410280	0.01045
NM_017866.6(TMEM70):c.684C>G (p.Asn228Lys)	rs35564486	0.00541
NM_017866.6(TMEM70):c.211-6C>T	rs113669789	0.00230
NM_017866.6(TMEM70):c.534T>C (p.Thr178=)	rs139864454	0.00136

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