List of variants in gene AFG3L2 reported as uncertain significance for optic atrophy

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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_006796.3(AFG3L2):c.2167G>A (p.Val723Met)	rs139469785	0.00024
NM_006796.3(AFG3L2):c.1762G>A (p.Ala588Thr)	rs374828650	0.00005
NM_006796.3(AFG3L2):c.2030T>C (p.Leu677Pro)	rs778455371	0.00002
NM_006796.3(AFG3L2):c.1013C>A (p.Ala338Glu)
NM_006796.3(AFG3L2):c.1714G>A (p.Ala572Thr)
NM_006796.3(AFG3L2):c.463G>A (p.Gly155Ser)	rs863223888

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