List of variants reported as uncertain significance for monogenic diabetes by Mendelics

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000545.8(HNF1A):c.1541A>G (p.His514Arg)	rs202039659	0.00028
NM_000545.8(HNF1A):c.716C>T (p.Ala239Val)	rs587778397	0.00016
NM_000162.5(GCK):c.836A>G (p.Glu279Gly)	rs143484733	0.00004
NM_000545.8(HNF1A):c.1522G>A (p.Glu508Lys)	rs483353044	0.00003
NM_000209.4(PDX1):c.97C>A (p.Pro33Thr)	rs192902098
NM_175914.5(HNF4A):c.944TGC[4] (p.Leu319del)	rs776489992

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