List of variants reported as benign for Joubert syndrome 3 by Illumina Laboratory Services, Illumina

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Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_001134831.2(AHI1):c.1780-14C>T	rs2757645	0.81825
NM_001134831.2(AHI1):c.3426+13G>A	rs6914831	0.59084
NM_017651.4(AHI1):c.-293G>T	rs13197384	0.29491
NM_001134831.2(AHI1):c.*218C>T	rs1052502	0.27386
NM_001134831.2(AHI1):c.-299G>A	rs113052089	0.03529
NM_001134831.2(AHI1):c.2223T>C (p.Asp741=)	rs2273761	0.02399
NM_001134831.2(AHI1):c.2488C>T (p.Arg830Trp)	rs13312995	0.02035
NM_001134831.2(AHI1):c.3053A>C (p.Gln1018Pro)	rs6940875	0.01691
NM_001134831.2(AHI1):c.3015A>G (p.Ser1005=)	rs41287054	0.01682
NM_001134831.2(AHI1):c.2624-6A>G	rs41288015	0.01635
NM_001134831.2(AHI1):c.1152-11T>G	rs113317693	0.01324
NM_001134831.2(AHI1):c.804A>C (p.Ser268=)	rs35528530	0.01078
NM_001134831.2(AHI1):c.1643G>A (p.Arg548His)	rs35433555	0.01070
NM_001134831.2(AHI1):c.3579T>C (p.Thr1193=)	rs115338154	0.00537
NM_001134831.2(AHI1):c.3368C>T (p.Ser1123Phe)	rs117447608	0.00497
NM_001134831.2(AHI1):c.517G>A (p.Ala173Thr)	rs146416468	0.00348
NM_001134831.2(AHI1):c.*28G>C	rs9494209

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