Related gene-specific medical variations for Gene (Select 4601) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2445390	NM_130439.3(MXI1):c.314C>T (p.Pro105Leu)	MXI1 (P105L +2 more)	Single nucleotide variant (missense variant)	Ovarian cancer	GLikely pathogenic
Select item 2445275	NM_130439.3(MXI1):c.343C>T (p.Pro115Ser)	MXI1 (P115S +2 more)	Single nucleotide variant (missense variant)	Ovarian cancer	GBenign
Select item 2218665	NM_130439.3(MXI1):c.13G>A (p.Gly5Arg)	LOC130004690, MXI1 (G5R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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