"Ambry Genetics"[submitter] AND "LOC130056344"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3314388	NM_024832.5(RIN3):c.278C>T (p.Ser93Leu)	LOC130056344, RIN3 (S93L +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2538362	NM_024832.5(RIN3):c.326C>T (p.Ser109Leu)	LOC130056344, RIN3 (S109L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance