List of variants reported as uncertain significance for monogenic diabetes by Institute of Human Genetics, University of Leipzig Medical Center

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000525.4(KCNJ11):c.526C>T (p.Arg176Cys)	rs201264306	0.00007
NM_000162.5(GCK):c.35A>G (p.Lys12Arg)	rs777958777	0.00001
NM_000162.5(GCK):c.529_530delinsTT (p.Glu177Leu)	rs2096278772
NM_000458.4(HNF1B):c.907C>T (p.Arg303Cys)	rs2033692513
NM_000458.4(HNF1B):c.908G>A (p.Arg303His)	rs2033692404
NM_001807.6(CEL):c.2031_2063dup (p.Gly688_Ala689insProProProValProProThrGlyAspSerGly)

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