"Constantin Polychronakos Laboratory, The Research Institute of the Mc - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 918067	NM_000207.3(INS):c.286T>C (p.Cys96Arg)	INS, INS-IGF2 (C96R)	Single nucleotide variant (missense variant +1 more)	Type 1 diabetes mellitus 2	GLikely risk allele
Select item 916729	NM_000207.3(INS):c.174del (p.Glu59fs)	INS, INS-IGF2 (E59fs)	Deletion (frameshift variant +1 more)	Neonatal insulin-dependent diabetes mellitus	GLikely pathogenic