"PreventionGenetics, part of Exact Sciences"[submitter] AND "LOC129996 - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3030337	NM_019096.5(GTPBP2):c.60C>T (p.Ala20=)	GTPBP2, LOC129996523 +1 more	Single nucleotide variant (synonymous variant +1 more)	GTPBP2-related disorder	GLikely benign
Select item 3037832	NM_019096.5(GTPBP2):c.21G>A (p.Glu7=)	GTPBP2, LOC129996523 +1 more	Single nucleotide variant (synonymous variant +1 more)	GTPBP2-related disorder	GLikely benign