List of variants reported as uncertain significance for Type 2 diabetes mellitus; Hyperinsulinism due to glucokinase deficiency; Maturity-onset diabetes of the young type 2; Permanent neonatal diabetes mellitus 1 by Fulgent Genetics, Fulgent Genetics

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Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_000162.5(GCK):c.646G>A (p.Glu216Lys)	rs778550411	0.00004
NM_000162.5(GCK):c.836A>G (p.Glu279Gly)	rs143484733	0.00004
NM_000162.5(GCK):c.301G>A (p.Val101Met)	rs762922697	0.00003
NM_000162.5(GCK):c.10G>A (p.Asp4Asn)	rs202091228	0.00002
NM_000162.5(GCK):c.394G>A (p.Asp132Asn)	rs762419802	0.00002
NM_000162.5(GCK):c.784G>A (p.Asp262Asn)	rs779460424	0.00002
NM_000162.5(GCK):c.107G>A (p.Arg36Gln)	rs193922261	0.00001
NM_000162.5(GCK):c.1386G>T (p.Met462Ile)	rs193922285	0.00001
NM_000162.5(GCK):c.415A>T (p.Met139Leu)	rs368137186	0.00001
NM_000162.5(GCK):c.951C>G (p.His317Gln)	rs1379908545	0.00001
NM_000162.5(GCK):c.1024A>C (p.Thr342Pro)	rs1000236360

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