"PreventionGenetics, part of Exact Sciences"[submitter] AND "LOC126859 - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 137288	NM_006567.5(FARS2):c.102G>A (p.Ser34=)	FARS2, LOC126859565	Single nucleotide variant (synonymous variant +1 more)	not specified +1 more	GBenign
Select item 260002	NM_006567.5(FARS2):c.183C>T (p.Asp61=)	FARS2, LOC126859565	Single nucleotide variant (synonymous variant +1 more)	not provided +2 more	GBenign
Select item 1109917	NM_006567.5(FARS2):c.213C>T (p.Leu71=)	FARS2, LOC126859565	Single nucleotide variant (synonymous variant +1 more)	Combined oxidative phosphorylation defect type 14 +1 more	GLikely benign
Select item 137289	NM_006567.5(FARS2):c.339C>T (p.Tyr113=)	FARS2, LOC126859565	Single nucleotide variant (synonymous variant +1 more)	Combined oxidative phosphorylation defect type 14 +1 more	GBenign
Select item 587651	NM_006567.5(FARS2):c.390C>A (p.Leu130=)	FARS2, LOC126859565	Single nucleotide variant (synonymous variant +1 more)	Combined oxidative phosphorylation defect type 14 +1 more	GLikely benign
Select item 1606582	NM_006567.5(FARS2):c.462G>A (p.Ala154=)	FARS2, LOC126859565	Single nucleotide variant (synonymous variant +1 more)	FARS2-related condition +1 more	GBenign/Likely benign
Select item 380526	NM_006567.5(FARS2):c.462G>T (p.Ala154=)	FARS2, LOC126859565	Single nucleotide variant (synonymous variant +1 more)	not provided +3 more	GBenign/Likely benign
Select item 214338	NM_006567.5(FARS2):c.506A>T (p.Asp169Val)	FARS2, LOC126859565 (D169V)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 2629582	NM_006567.5(FARS2):c.509C>T (p.Ala170Val)	FARS2, LOC126859565 (A170V)	Single nucleotide variant (missense variant +1 more)	FARS2-related condition	GUncertain significance