"MGZ Medical Genetics Center"[submitter] AND "INS"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 253331	NM_000207.3(INS):c.125T>C (p.Val42Ala)	INS, INS-IGF2 (V42A)	Single nucleotide variant (missense variant +1 more)	Maturity-onset diabetes of the young type 10 +1 more	GConflicting classifications of pathogenicity
Select item 1317682	NM_000207.3(INS):c.-153C>G	INS	Single nucleotide variant	not specified +5 more	GConflicting classifications of pathogenicity