Related gene-specific medical variations for Gene (Select 4099) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1341703	NM_002361.4(MAG):c.562C>T (p.Arg188Trp)	MAG (R163W +1 more)	Single nucleotide variant (missense variant)	Hereditary spastic paraplegia 75	GUncertain significance
Select item 808512	NM_002361.4(MAG):c.34A>G (p.Ile12Val)	MAG (I12V)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 548561	NM_002361.4(MAG):c.1324G>A (p.Val442Met)	MAG (V442M +1 more)	Single nucleotide variant (missense variant)	Hereditary spastic paraplegia 75	GUncertain significance

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