List of variants reported as uncertain significance for Renal cysts and diabetes syndrome; Type 2 diabetes mellitus; Nonpapillary renal cell carcinoma by Fulgent Genetics, Fulgent Genetics

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Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_000458.4(HNF1B):c.1207A>T (p.Ile403Phe)	rs747110790	0.00003
NM_000458.4(HNF1B):c.1390G>A (p.Gly464Ser)	rs982085453	0.00002
NM_000458.4(HNF1B):c.314A>G (p.Glu105Gly)	rs375625110	0.00002
NM_000458.4(HNF1B):c.1117G>A (p.Ala373Thr)	rs759270956	0.00001
NM_000458.4(HNF1B):c.1305G>T (p.Met435Ile)	rs1199229728	0.00001
NM_000458.4(HNF1B):c.592A>C (p.Ser198Arg)	rs1321074352	0.00001
NM_000458.4(HNF1B):c.107C>T (p.Ser36Phe)
NM_000458.4(HNF1B):c.140C>T (p.Pro47Leu)
NM_000458.4(HNF1B):c.1657C>A (p.Pro553Thr)
NM_000458.4(HNF1B):c.578T>C (p.Met193Thr)	rs760079000
NM_000458.4(HNF1B):c.754C>T (p.Arg252Trp)	rs748416956

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