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

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3026167	NM_003011.4(SET):c.225C>T (p.Ile75=)	SET	Single nucleotide variant (synonymous variant)	SET-related disorder +1 more	GLikely benign
Select item 2631229	NM_003011.4(SET):c.587A>G (p.His196Arg)	SET (H185R +3 more)	Single nucleotide variant (missense variant)	SET-related disorder	GUncertain significance
Select item 3044296	NM_003011.4(SET):c.591T>C (p.Ser197=)	SET	Single nucleotide variant (synonymous variant)	SET-related disorder	GLikely benign
Select item 3045766	NM_003011.4(SET):c.664-5_664-4del	SET	Deletion (intron variant)	SET-related disorder	GLikely benign
Select item 3046681	NM_003011.4(SET):c.702A>T (p.Glu234Asp)	SET (E223D +3 more)	Single nucleotide variant (missense variant)	SET-related disorder	GLikely benign

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