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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1801851	NM_000207.3(INS):c.153A>C (p.Thr51=)	INS, INS-IGF2	Single nucleotide variant (synonymous variant +1 more)	Inborn genetic diseases +2 more	GBenign/Likely benign
Select item 1774163	NM_000207.3(INS):c.150C>T (p.Tyr50=)	INS, INS-IGF2	Single nucleotide variant (synonymous variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2284265	NM_001042376.3(INS-IGF2):c.145T>C (p.Phe49Leu)	INS, INS-IGF2 (F49L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 880304	NM_000207.3(INS):c.72C>A (p.Ala24=)	INS, INS-IGF2	Single nucleotide variant (synonymous variant +1 more)	Transient Neonatal Diabetes, Dominant/Recessive +4 more	GBenign/Likely benign
Select item 255533	NM_000207.3(INS):c.63A>G (p.Pro21=)	INS, INS-IGF2	Single nucleotide variant (synonymous variant +1 more)	Maturity-onset diabetes of the young type 10 +3 more	GConflicting classifications of pathogenicity
Select item 2311109	NM_001042376.3(INS-IGF2):c.52G>C (p.Gly18Arg)	INS, INS-IGF2 (G18R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar