Related gene-specific medical variations for Gene (Select 63899) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3247039	NC_000003.11:g.(?_93802931)_(93803314_?)del	NSUN3	Deletion	not provided	GUncertain significance
Select item 3001997	NM_022072.5(NSUN3):c.4C>G (p.Leu2Val)	DHFR2, LOC129937100 +1 more (L2V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2964336	NM_022072.5(NSUN3):c.1A>G (p.Met1Val)	DHFR2, LOC129937100 +1 more (M1V)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance

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