"PreventionGenetics, part of Exact Sciences"[submitter] AND "SPRY2"[ge - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2630300	NM_005842.4(SPRY2):c.893_894del (p.Thr298fs)	SPRY2 (T298fs)	Microsatellite (frameshift variant)	SPRY2-related condition	GUncertain significance
Select item 3029049	NM_005842.4(SPRY2):c.870T>C (p.Gly290=)	SPRY2	Single nucleotide variant (synonymous variant)	SPRY2-related condition	GLikely benign
Select item 3040976	NM_005842.4(SPRY2):c.426C>T (p.Ser142=)	SPRY2	Single nucleotide variant (synonymous variant)	SPRY2-related condition	GBenign

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