List of variants in gene combination AIFM1, RAB33A reported as likely pathogenic 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.1006G>A (p.Glu336Lys)	rs1603223158
NM_004208.4(AIFM1):c.1020G>T (p.Met340Ile)
NM_004208.4(AIFM1):c.1195G>A (p.Gly399Ser)
NM_004208.4(AIFM1):c.1424C>T (p.Pro475Leu)	rs724160022

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