ClinVar Miner

List of variants in gene HNF1B reported as benign for not provided

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Gene type:
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Total variants: 46
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HGVS dbSNP gnomAD frequency
NM_000458.4(HNF1B):c.1340-115= rs2074429 0.82029
NM_000458.4(HNF1B):c.*100= rs1555818000 0.80645
NM_000458.4(HNF1B):c.1654-22= rs3110641 0.67606
NM_000458.4(HNF1B):c.*274= rs2689 0.38166
NM_000458.4(HNF1B):c.1535-177T>C rs2269841 0.34224
NM_000458.4(HNF1B):c.1535-225_1535-224insC rs11440398 0.34179
NM_000458.4(HNF1B):c.1535-185G>C rs12938438 0.29614
NM_000458.4(HNF1B):c.1535-46T>G rs2269842 0.29082
NM_000458.4(HNF1B):c.*99C>A rs2229295 0.27047
NM_000458.4(HNF1B):c.1045+330G>C rs9906451 0.18495
NM_000458.4(HNF1B):c.1653+47_1653+48insC rs35913775 0.16032
NM_000458.4(HNF1B):c.1339+27T>C rs2107133 0.08783
NM_000458.4(HNF1B):c.1340-100C>T rs9905004 0.08731
NM_000458.4(HNF1B):c.1654-106C>T rs8066605 0.08136
NM_000458.4(HNF1B):c.1535-102A>G rs13339672 0.06851
NM_000458.4(HNF1B):c.1534+252G>C rs72830475 0.06206
NM_000458.4(HNF1B):c.344+256G>C rs111950175 0.06108
NM_000458.4(HNF1B):c.344+228G>C rs113656333 0.06093
NM_000458.4(HNF1B):c.345-228C>G rs75979306 0.06037
NC_000017.11:g.37745441C>T rs78856518 0.02990
NM_000458.4(HNF1B):c.*47T>G rs8068014 0.02908
NM_000458.4(HNF1B):c.1653+89G>A rs9890418 0.02843
NM_000458.4(HNF1B):c.1534+105A>G rs2189302 0.02651
NM_000458.4(HNF1B):c.1340-97G>A rs77297671 0.01990
NM_000458.4(HNF1B):c.345-19C>T rs59527848 0.00765
NM_000458.4(HNF1B):c.1413C>T (p.Pro471=) rs140781855 0.00325
NM_000458.4(HNF1B):c.444G>A (p.Ser148=) rs147218489 0.00228
NM_000458.4(HNF1B):c.951C>G (p.Ala317=) rs145750370 0.00127
NM_000458.4(HNF1B):c.1045+12T>C rs141166864 0.00097
NM_000458.4(HNF1B):c.852C>T (p.His284=) rs149581999 0.00022
NM_000458.4(HNF1B):c.73G>T (p.Val25Leu) rs139107479 0.00015
NM_000458.4(HNF1B):c.1373T>G (p.Val458Gly) rs375644184 0.00002
NM_000458.4(HNF1B):c.1006C>A (p.His336Asn) rs138986885
NM_000458.4(HNF1B):c.1046-279G>A rs7225211
NM_000458.4(HNF1B):c.1046-4308=
NM_000458.4(HNF1B):c.1134G>A (p.Gln378=)
NM_000458.4(HNF1B):c.1207-247_1207-246insGG rs10701156
NM_000458.4(HNF1B):c.1474G>A (p.Gly492Ser)
NM_000458.4(HNF1B):c.182T>G (p.Val61Gly)
NM_000458.4(HNF1B):c.344+65T>G rs111699857
NM_000458.4(HNF1B):c.344+967=
NM_000458.4(HNF1B):c.345-1956=
NM_000458.4(HNF1B):c.345-210=
NM_000458.4(HNF1B):c.544+1391=
NM_000458.4(HNF1B):c.544+14T>A rs759120365
NM_000458.4(HNF1B):c.810-40G>C rs150712273

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