List of variants in gene combination AIFM1, LOC130068679, RAB33A reported as benign for Charcot-Marie-Tooth Neuropathy X; Combined oxidative phosphorylation deficiency

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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_004208.4(AIFM1):c.103C>T (p.Pro35Ser)	rs61730896	0.00489
NM_004208.4(AIFM1):c.106+15C>G	rs199863662	0.00059
NM_004208.4(AIFM1):c.72C>T (p.Cys24=)	rs373609902	0.00051
NM_004208.4(AIFM1):c.54C>G (p.Pro18=)	rs140076585	0.00049

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