List of variants reported as likely benign for Meckel syndrome, type 6; Joubert syndrome 9; COACH syndrome 2; Retinitis pigmentosa 93 by Fulgent Genetics, Fulgent Genetics

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001378615.1(CC2D2A):c.2181+7A>C	rs143681243	0.00124
NM_001378615.1(CC2D2A):c.1691C>T (p.Thr564Met)	rs201954181	0.00026
NM_001378615.1(CC2D2A):c.4675-15G>A	rs377573053	0.00026
NM_001378615.1(CC2D2A):c.603C>T (p.Pro201=)	rs556542553	0.00011
NM_001378615.1(CC2D2A):c.786C>T (p.Asp262=)	rs200434902	0.00009

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