"Fulgent Genetics, Fulgent Genetics"[submitter] AND "INS-IGF2"[gene] - ClinVar - NCBI

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Items: 8

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 976061	NM_000612.6(IGF2):c.100G>T (p.Gly34Cys)	IGF2, INS-IGF2 (G34C +1 more)	Single nucleotide variant (missense variant +1 more)	Silver-Russell syndrome 3 +3 more	GLikely pathogenic
Select item 129279	NM_000207.3(INS):c.188-10G>A	INS, INS-IGF2	Single nucleotide variant (intron variant)	Neonatal insulin-dependent diabetes mellitus +8 more	GBenign/Likely benign
Select item 36400	NM_000207.3(INS):c.188-16C>T	INS, INS-IGF2	Single nucleotide variant (intron variant)	Neonatal diabetes mellitus +7 more	GBenign/Likely benign
Select item 255532	NM_000207.3(INS):c.187+11T>C	INS, INS-IGF2 +1 more	Single nucleotide variant (intron variant)	Maturity-onset diabetes of the young type 10 +8 more	GBenign/Likely benign
Select item 730224	NM_000207.3(INS):c.67G>A (p.Ala23Thr)	INS, INS-IGF2 (A23T)	Single nucleotide variant (missense variant +1 more)	not provided +7 more	GConflicting classifications of pathogenicity
Select item 304057	NM_000207.3(INS):c.36G>A (p.Ala12=)	INS, INS-IGF2 +1 more	Single nucleotide variant (synonymous variant +1 more)	Maturity-onset diabetes of the young type 10 +7 more	GBenign/Likely benign
Select item 304058	NM_000207.3(INS):c.25C>T (p.Pro9Ser)	INS, INS-IGF2 (P9S)	Single nucleotide variant (missense variant +1 more)	Maturity-onset diabetes of the young type 10 +6 more	GUncertain significance
Select item 1455986	NM_000207.3(INS):c.1A>G (p.Met1Val)	INS, INS-IGF2 (M1V)	Single nucleotide variant (missense variant +2 more)	Type 1 diabetes mellitus 2 +4 more	GPathogenic/Likely pathogenic