"PreventionGenetics, part of Exact Sciences"[submitter] AND "RIC1"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3036783	NM_020829.4(RIC1):c.145-9del	RIC1	Deletion (intron variant)	RIC1-related disorder	GLikely benign
Select item 3053964	NM_020829.4(RIC1):c.1051A>G (p.Arg351Gly)	RIC1 (R351G)	Single nucleotide variant (missense variant)	RIC1-related disorder	GLikely benign
Select item 3046510	NM_020829.4(RIC1):c.1328C>G (p.Pro443Arg)	RIC1 (P443R)	Single nucleotide variant (missense variant)	RIC1-related disorder	GLikely benign
Select item 3047542	NM_020829.4(RIC1):c.1808C>G (p.Ala603Gly)	RIC1 (A566G +1 more)	Single nucleotide variant (missense variant)	RIC1-related disorder	GLikely benign
Select item 3041454	NM_020829.4(RIC1):c.3424+70A>G	RIC1 (Y1165C)	Single nucleotide variant (missense variant +1 more)	RIC1-related disorder	GLikely benign
Select item 3024888	NM_020829.4(RIC1):c.3611A>G (p.Asn1204Ser)	RIC1 (N1167S +1 more)	Single nucleotide variant (missense variant)	RIC1-related disorder +1 more	GLikely benign
Select item 3051868	NM_020829.4(RIC1):c.4203GGA[1] (p.Glu1402del)	RIC1 (E1365del +1 more)	Microsatellite (inframe deletion)	RIC1-related disorder	GLikely benign

ClinVar