ClinVar for MedGen (Select 852189) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 255531	NM_000207.3(INS):c.*9C>T	INS, INS-IGF2 +1 more	Single nucleotide variant (3 prime UTR variant +1 more)	Maturity-onset diabetes of the young type 10 +5 more	GBenign/Likely benign
Select item 129763	NM_002500.5(NEUROD1):c.590C>A (p.Pro197His)	NEUROD1 (P197H)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity