List of variants in gene combination AIFM1, RAB33A reported as uncertain significance for Charcot-Marie-Tooth disease

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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
NM_004208.4(AIFM1):c.1597G>A (p.Glu533Lys)	rs1057517852
NM_004208.4(AIFM1):c.1627A>G (p.Ile543Val)	rs0
NM_004208.4(AIFM1):c.513G>A (p.Met171Ile)	rs0
NM_004208.4(AIFM1):c.602G>A (p.Arg201Lys)	rs886703882

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