List of variants in gene combination AIFM1, RAB33A reported as uncertain significance for peripheral neuropathy

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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: 17

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HGVS	dbSNP	gnomAD frequency
NM_004208.4(AIFM1):c.170C>G (p.Ser57Cys)	rs201711375	0.00010
NM_004208.4(AIFM1):c.1627A>G (p.Ile543Val)	rs1175521163	0.00006
NM_004208.4(AIFM1):c.1597G>A (p.Glu533Lys)	rs1057517852	0.00004
NM_004208.4(AIFM1):c.1646C>T (p.Ala549Val)	rs761953453	0.00001
NM_004208.4(AIFM1):c.1693A>G (p.Ile565Val)	rs1375125488	0.00001
NM_004208.4(AIFM1):c.1006G>A (p.Glu336Lys)	rs1603223158
NM_004208.4(AIFM1):c.1019T>C (p.Met340Thr)	rs1057518895
NM_004208.4(AIFM1):c.1241T>C (p.Ile414Thr)	rs1603222490
NM_004208.4(AIFM1):c.1478A>T (p.Glu493Val)	rs281864468
NM_004208.4(AIFM1):c.322CAGAAA[1] (p.108QK[1])	rs2030881306
NM_004208.4(AIFM1):c.511A>C (p.Met171Leu)
NM_004208.4(AIFM1):c.513G>A (p.Met171Ile)	rs2030801103
NM_004208.4(AIFM1):c.602G>A (p.Arg201Lys)	rs886703882
NM_004208.4(AIFM1):c.623C>T (p.Pro208Leu)
NM_004208.4(AIFM1):c.727G>T (p.Val243Leu)	rs1603225138
NM_004208.4(AIFM1):c.923G>A (p.Gly308Glu)	rs1603224226
NM_004208.4(AIFM1):c.994C>G (p.Gln332Glu)	rs2124653092

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