Related gene-specific medical variations for Gene (Select 8480) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3217804	NM_003610.4(RAE1):c.288+2453C>G	MTRNR2L3, RAE1	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 3217798	NM_003610.4(RAE1):c.288+2479C>T	MTRNR2L3, RAE1	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 2518063	NM_003610.4(RAE1):c.288+2455A>G	MTRNR2L3, RAE1	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 2466679	NM_003610.4(RAE1):c.288+2455A>T	MTRNR2L3, RAE1	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 2465026	NM_003610.4(RAE1):c.288+2444C>T	MTRNR2L3, RAE1	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 2391807	NM_003610.4(RAE1):c.288+2434C>T	MTRNR2L3, RAE1	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 2384654	NM_003610.4(RAE1):c.288+2497G>T	MTRNR2L3, RAE1	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 2384653	NM_003610.4(RAE1):c.288+2498C>T	MTRNR2L3, RAE1	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 91952	NM_003610.4(RAE1):c.408C>G (p.Ile136Met)	RAE1 (I136M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

ClinVar