Related gene-specific medical variations for Gene (Select 9603) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3299520	NM_004289.7(NFE2L3):c.1985A>G (p.Tyr662Cys)	LOC129998143, NFE2L3 (Y662C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197371	NM_004289.7(NFE2L3):c.2007T>A (p.Asp669Glu)	LOC129998143, NFE2L3 (D669E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197366	NM_004289.7(NFE2L3):c.1888G>T (p.Ala630Ser)	LOC129998142, NFE2L3 (A630S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2657357	NM_004289.7(NFE2L3):c.2035C>T (p.Leu679=)	LOC129998143, NFE2L3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2523815	NM_004289.7(NFE2L3):c.2050C>T (p.His684Tyr)	LOC129998143, NFE2L3 (H684Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 493559	GRCh37/hg19 7p15.2(chr7:26086266-26223793)x3	NFE2L3	Copy number gain	not provided	GLikely benign

ClinVar