List of variants reported as uncertain significance for Joubert syndrome 3 by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001134831.2(AHI1):c.1694G>A (p.Arg565His)	rs372894716	0.00007
NM_001134831.2(AHI1):c.2501C>T (p.Ala834Val)	rs529407899	0.00001
NM_001134831.2(AHI1):c.1829G>C (p.Arg610Pro)	rs374009466
NM_001134831.2(AHI1):c.928G>A (p.Ala310Thr)	rs2484971821

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