Related gene-specific medical variations for Gene (Select 29924) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3089756	NM_001130072.2(EPN1):c.-101-813C>T	EPN1, LOC125384546 (P71L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2650541	NM_176820.4(NLRP9):c.2943C>T (p.Asp981=)	EPN1, NLRP9	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GLikely benign
Select item 2348971	NM_176820.4(NLRP9):c.2944G>A (p.Glu982Lys)	EPN1, NLRP9 (E982K)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance

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