C0011860[trait identifier] AND "Center for Genomic Medicine, King Fais - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 342923	NM_138711.6(PPARG):c.391-3C>T	PPARG	Single nucleotide variant (intron variant)	Obesity +4 more	GConflicting classifications of pathogenicity
Select item 211076	NM_000162.5(GCK):c.835G>C (p.Glu279Gln)	GCK (E279Q +2 more)	Single nucleotide variant (missense variant)	Monogenic diabetes	GBenign FDA Recognized database
Select item 3064083	NM_173851.3(SLC30A8):c.592C>T (p.Gln198Ter)	SLC30A8 (Q149* +1 more)	Single nucleotide variant (nonsense)	Type 2 diabetes mellitus	GUncertain significance
Select item 1219242	NM_000525.4(KCNJ11):c.101G>A (p.Arg34His)	KCNJ11 (R34H)	Single nucleotide variant (missense variant +1 more)	Type 2 diabetes mellitus +5 more	GPathogenic/Likely pathogenic
Select item 551999	NM_000352.6(ABCC8):c.4412-13G>A	ABCC8	Single nucleotide variant (intron variant)	not provided +3 more	GPathogenic/Likely pathogenic
Select item 9086	NM_000352.6(ABCC8):c.4307G>A (p.Arg1436Gln)	ABCC8 (R1436Q +3 more)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GPathogenic
Select item 370722	NM_000352.6(ABCC8):c.4021C>T (p.Gln1341Ter)	ABCC8 (Q1341* +3 more)	Single nucleotide variant (nonsense +1 more)	Type 2 diabetes mellitus +4 more	GConflicting classifications of pathogenicity

ClinVar