ClinVar (all) for Orgtrack (Select 508397) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 946956	NM_021930.6(RINT1):c.1021C>G (p.Leu341Val)	RINT1 (L33V +2 more)	Single nucleotide variant (missense variant +2 more)	Thyroid cancer, nonmedullary, 1 +2 more	GConflicting classifications of pathogenicity
Select item 653869	NM_021930.6(RINT1):c.1107+1G>T	RINT1	Single nucleotide variant (splice donor variant)	not provided +1 more	GLikely pathogenic