C3809369[trait identifier] AND "Institute for Medical Genetics and Hum - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 548927	NM_015937.6(PIGT):c.197del (p.Tyr66fs)	PIGT (Y66fs)	Deletion (frameshift variant +2 more)	Paroxysmal nocturnal hemoglobinuria 2	Grisk factor
Select item 599265	NM_015937.6(PIGT):c.767_770del (p.Lys256fs)	PIGT (K256fs +2 more)	Microsatellite (frameshift variant +1 more)	Paroxysmal nocturnal hemoglobinuria 2	Grisk factor