Related gene-specific medical variations for Gene (Select 84245) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2689445	NM_001031727.4(MRI1):c.363_371+2del	MRI1	Deletion (splice donor variant)	not provided	GUncertain significance
Select item 2689444	NM_001031727.4(MRI1):c.722C>G (p.Ser241Ter)	MRI1 (S194* +2 more)	Single nucleotide variant (nonsense +1 more)	not provided	GUncertain significance
Select item 2463387	NM_001031727.4(MRI1):c.154G>T (p.Ala52Ser)	LOC130063724, MRI1 (A52S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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