List of variants reported as uncertain significance for Joubert syndrome 15 by Fulgent Genetics, Fulgent Genetics

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_018718.3(CEP41):c.107T>C (p.Met36Thr)	rs368178632	0.00011
NM_018718.3(CEP41):c.725G>A (p.Arg242His)	rs191246968	0.00003
NM_018718.3(CEP41):c.1087A>G (p.Ser363Gly)	rs201504407	0.00001
NM_018718.3(CEP41):c.28C>G (p.Pro10Ala)	rs149373377

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