List of variants reported as uncertain significance for Multiple mitochondrial dysfunctions syndrome 3

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001010867.4(IBA57):c.574G>A (p.Ala192Thr)	rs140163897	0.00034
NM_001010867.4(IBA57):c.679+3A>G	rs754620334	0.00006
NM_001010867.4(IBA57):c.266C>T (p.Pro89Leu)	rs1191467500	0.00001
NM_001010867.4(IBA57):c.826C>T (p.Arg276Cys)	rs143575106	0.00001
NM_001010867.4(IBA57):c.827G>A (p.Arg276His)	rs1245306816	0.00001
NM_001010867.4(IBA57):c.724C>T (p.Pro242Ser)	rs923591178
NM_001010867.4(IBA57):c.778T>C (p.Tyr260His)

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