Related gene-specific medical variations for Gene (Select 79917) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3122299	NM_024859.4(MAGIX):c.854C>G (p.Pro285Arg)	LOC119407416, MAGIX (P226R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122298	NM_024859.4(MAGIX):c.65C>G (p.Pro22Arg)	LOC130068275, MAGIX (P22R)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2599382	NM_024859.4(MAGIX):c.101G>T (p.Arg34Leu)	LOC130068275, MAGIX (R34L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2489723	NM_024859.4(MAGIX):c.917C>T (p.Pro306Leu)	LOC119407416, MAGIX (P225L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2406633	NM_024859.4(MAGIX):c.50G>A (p.Gly17Asp)	LOC130068275, MAGIX (G17D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2224783	NM_024859.4(MAGIX):c.875C>T (p.Pro292Leu)	LOC119407416, MAGIX (P211L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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