"PreventionGenetics, part of Exact Sciences"[submitter] AND "LOC129935 - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3043609	NM_014905.5(GLS):c.266A>C (p.His89Pro)	GLS, LOC129935270 (H89P)	Single nucleotide variant (missense variant)	GLS-related disorder	GBenign
Select item 2634709	NM_014905.5(GLS):c.286C>T (p.Pro96Ser)	GLS, LOC129935270 (P96S)	Single nucleotide variant (missense variant)	GLS-related disorder	GUncertain significance
Select item 3054890	NM_014905.5(GLS):c.290C>T (p.Pro97Leu)	GLS, LOC129935270 (P97L)	Single nucleotide variant (missense variant)	GLS-related disorder	GLikely benign

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