AIFM1[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3245679	NC_000023.10:g.(?_129290415)_(129290597_?)dup	AIFM1	Duplication	Charcot-Marie-Tooth Neuropathy X +1 more	GUncertain significance
Select item 2425040	NC_000023.10:g.(?_129263532)_(129272696_?)dup	AIFM1	Duplication	Charcot-Marie-Tooth Neuropathy X +1 more	GUncertain significance
Select item 2425039	NC_000023.10:g.(?_129263532)_(129299630_?)dup	AIFM1	Duplication	Combined oxidative phosphorylation deficiency +1 more	GUncertain significance
Select item 2425038	NC_000023.10:g.(?_129263532)_(129299630_?)del	AIFM1	Deletion	Combined oxidative phosphorylation deficiency +1 more	GUncertain significance

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