List of variants reported as uncertain significance for Joubert syndrome 3 by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 3

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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.2560T>C (p.Cys854Arg)	rs1387769677	0.00002
NM_001134831.2(AHI1):c.1933C>T (p.Arg645Cys)	rs1291908829	0.00001

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