"PreventionGenetics, part of Exact Sciences"[submitter] AND "ARMS2"[ge - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 299029	NM_001099667.3(ARMS2):c.112C>T (p.Arg38Ter)	ARMS2 (R38*)	Single nucleotide variant (nonsense)	ARMS2-related disorder +1 more	GBenign/Likely benign
Select item 979	NM_001099667.3(ARMS2):c.205G>T (p.Ala69Ser)	ARMS2 (A69S)	Single nucleotide variant (missense variant)	ARMS2-related disorder +2 more	GBenign