List of variants reported as uncertain significance for Renal cysts and diabetes syndrome by Illumina Laboratory Services, Illumina

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Total variants: 25

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HGVS	dbSNP	gnomAD frequency
NM_000458.4(HNF1B):c.*625C>T	rs188957129	0.00154
NM_000458.4(HNF1B):c.*691A>G	rs751817675	0.00064
NM_000458.4(HNF1B):c.*445A>G	rs571607314	0.00029
NM_000458.4(HNF1B):c.*629C>T	rs566057658	0.00026
NM_000458.4(HNF1B):c.*701G>A	rs886052888	0.00015
NM_000458.4(HNF1B):c.-82G>T	rs886052892	0.00013
NM_000458.4(HNF1B):c.36C>T (p.Leu12=)	rs749370057	0.00006
NM_000458.4(HNF1B):c.1207A>T (p.Ile403Phe)	rs747110790	0.00003
NM_000458.4(HNF1B):c.9C>T (p.Ser3=)	rs773256244	0.00003
NM_000458.4(HNF1B):c.*789T>C	rs886052887	0.00001
NM_000458.4(HNF1B):c.268C>A (p.Pro90Thr)	rs772315985	0.00001
NM_000458.4(HNF1B):c.96G>A (p.Glu32=)	rs778229703	0.00001
NM_000458.4(HNF1B):c.*409A>G	rs2031989734
NM_000458.4(HNF1B):c.*585T>C	rs886052889
NM_000458.4(HNF1B):c.-36del	rs756559188
NM_000458.4(HNF1B):c.1395C>G (p.Ser465Arg)
NM_000458.4(HNF1B):c.1418A>G (p.Gln473Arg)	rs886052891
NM_000458.4(HNF1B):c.150T>G (p.Pro50=)	rs2034119944
NM_000458.4(HNF1B):c.1654-11T>C	rs193922484
NM_000458.4(HNF1B):c.1654-14CT[4]	rs886052890
NM_000458.4(HNF1B):c.309G>C (p.Ala103=)	rs1197263675
NM_000458.4(HNF1B):c.438C>T (p.Asn146=)	rs2033930573
NM_000458.4(HNF1B):c.477T>C (p.Pro159=)	rs1212716750
NM_000458.4(HNF1B):c.517G>A (p.Val173Ile)
NM_000458.4(HNF1B):c.928C>T (p.Arg310Trp)	rs988279557

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