ClinVar Miner

List of variants reported as benign for Renal cysts and diabetes syndrome

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Total variants: 25
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HGVS dbSNP gnomAD frequency
NM_000458.4(HNF1B):c.*100= rs1555818000 0.80645
NM_000458.4(HNF1B):c.1654-22= rs3110641 0.67606
NM_000458.4(HNF1B):c.*444= rs2688 0.58526
NM_000458.4(HNF1B):c.*274= rs2689 0.38166
NM_000458.4(HNF1B):c.*99C>A rs2229295 0.27047
NM_000458.4(HNF1B):c.*924C>G rs10962 0.22156
NM_000458.4(HNF1B):c.*384A>G rs1058166 0.17933
NM_000458.4(HNF1B):c.*777G>A rs17138512 0.02929
NM_000458.4(HNF1B):c.*47T>G rs8068014 0.02908
NM_000458.4(HNF1B):c.*804T>C rs75361710 0.01316
NM_000458.4(HNF1B):c.345-19C>T rs59527848 0.00765
NM_000458.4(HNF1B):c.-67C>T rs140699244 0.00491
NM_000458.4(HNF1B):c.*659G>A rs182736930 0.00215
NM_016203.4(PRKAG2):c.298G>A (p.Gly100Ser) rs79474211 0.00144
NM_000458.4(HNF1B):c.*683G>A rs144234352 0.00126
NM_000458.4(HNF1B):c.1045+12T>C rs141166864 0.00097
NM_000458.4(HNF1B):c.*403A>G rs557216745 0.00016
NM_000458.4(HNF1B):c.1373T>G (p.Val458Gly) rs375644184 0.00002
NM_000458.4(HNF1B):c.*938A>G rs574000398
NM_000458.4(HNF1B):c.-31C>G rs771697321
NM_000458.4(HNF1B):c.1006C>G (p.His336Asp)
NM_000458.4(HNF1B):c.182T>G (p.Val61Gly)
NM_000458.4(HNF1B):c.244G>A (p.Asp82Asn)
NM_000458.4(HNF1B):c.345-4C>T rs200590728
NM_000458.4(HNF1B):c.657C>T (p.Ser219=) rs148713761

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