C4225250[trait identifier] AND "OMIM"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 218187	NM_002361.4(MAG):c.399C>G (p.Ser133Arg)	MAG (S133R +1 more)	Single nucleotide variant (missense variant)	Hereditary spastic paraplegia 75	GPathogenic
Select item 120188	NM_002361.4(MAG):c.1288T>G (p.Cys430Gly)	MAG (C430G +1 more)	Single nucleotide variant (missense variant)	Hereditary spastic paraplegia 75	GPathogenic