List of variants reported as uncertain significance for combined oxidative phosphorylation deficiency by Undiagnosed Diseases Network, NIH

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_020442.6(VARS2):c.1168G>A (p.Ala390Thr)	rs202201763	0.00039
NM_005932.4(MIPEP):c.485T>G (p.Leu162Trp)	rs768628283	0.00001
NM_020442.6(VARS2):c.842G>A (p.Cys281Tyr)
NM_020442.6(VARS2):c.986-14A>G	rs1297230026

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