"New York Genome Center"[submitter] AND "INS-IGF2"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1049511	NM_000207.3(INS):c.227G>A (p.Ser76Asn)	INS, INS-IGF2 (S76N)	Single nucleotide variant (missense variant +1 more)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 304058	NM_000207.3(INS):c.25C>T (p.Pro9Ser)	INS, INS-IGF2 (P9S)	Single nucleotide variant (missense variant +1 more)	INS-related condition +6 more	GUncertain significance