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

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3047154	NM_173849.3(GSC):c.228C>A (p.Ser76=)	GSC	Single nucleotide variant (synonymous variant)	GSC-related disorder	GLikely benign
Select item 783695	NM_173849.3(GSC):c.214G>A (p.Ala72Thr)	GSC (A72T)	Single nucleotide variant (missense variant)	GSC-related disorder +1 more	GBenign