"Ambry Genetics"[submitter] AND "WARS2-AS1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2407993	NM_015836.4(WARS2):c.90+2T>A	LOC129931299, WARS2 +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3189511	NM_015836.4(WARS2):c.48C>G (p.Ile16Met)	LOC129931299, WARS2 +1 more (I16M)	Single nucleotide variant (non-coding transcript variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2336895	NM_015836.4(WARS2):c.46A>T (p.Ile16Phe)	LOC129931299, WARS2 +1 more (I16F)	Single nucleotide variant (non-coding transcript variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 1947813	NM_015836.4(WARS2):c.37T>C (p.Trp13Arg)	LOC129931299, WARS2 +1 more (W13R)	Single nucleotide variant (non-coding transcript variant +2 more)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 440915	NM_015836.4(WARS2):c.37T>G (p.Trp13Gly)	LOC129931299, WARS2 +1 more (W13G)	Single nucleotide variant (missense variant +2 more)	WARS2-Related Disorders +6 more	GConflicting classifications of pathogenicity
Select item 2283912	NM_015836.4(WARS2):c.24A>T (p.Lys8Asn)	LOC129931299, WARS2 +1 more (K8N)	Single nucleotide variant (non-coding transcript variant +2 more)	Inborn genetic diseases	GUncertain significance

ClinVar