"PreventionGenetics, part of Exact Sciences"[submitter] AND "RASIP1"[g - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3044744	NM_017805.3(RASIP1):c.2827G>A (p.Asp943Asn)	LOC117125599, RASIP1 (D943N)	Single nucleotide variant (missense variant)	RASIP1-related disorder	GLikely benign
Select item 3043743	NM_017805.3(RASIP1):c.2527C>T (p.Arg843Cys)	RASIP1 (R843C)	Single nucleotide variant (missense variant)	RASIP1-related disorder	GLikely benign