Related gene-specific medical variations for Gene (Select 25793) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3247743	NC_000022.10:g.(?_32891460)_(32894517_?)del	FBXO7	Deletion	Parkinsonian-pyramidal syndrome	GPathogenic
Select item 3247732	NC_000022.10:g.(?_32894111)_(32894517_?)del	FBXO7	Deletion	Parkinsonian-pyramidal syndrome	GPathogenic
Select item 433543	NM_012179.4(FBXO7):c.520T>A (p.Ser174Thr)	FBXO7 (S174T +2 more)	Single nucleotide variant (missense variant)	Not Specified	Gno classification for the single variant Sno classification for the single variant Ono classification for the single variant

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