ClinVar Miner

List of variants in gene HNF1B reported as likely benign for pancreas disorder

Included ClinVar conditions (165):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 78
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HGVS dbSNP gnomAD frequency
NM_000458.4(HNF1B):c.344+256G>C rs111950175 0.06108
NM_000458.4(HNF1B):c.*777G>A rs17138512 0.02929
NM_000458.4(HNF1B):c.1340-97G>A rs77297671 0.01990
NM_000458.4(HNF1B):c.*804T>C rs75361710 0.01316
NM_000458.4(HNF1B):c.1340-303T>A rs112298654 0.01150
NM_000458.3(HNF1B):c.-178G>A rs148442901 0.00528
NM_000458.4(HNF1B):c.-67C>T rs140699244 0.00491
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.*659G>A rs182736930 0.00215
NM_000458.4(HNF1B):c.*625C>T rs188957129 0.00154
NM_000458.4(HNF1B):c.951C>G (p.Ala317=) rs145750370 0.00127
NM_000458.4(HNF1B):c.*683G>A rs144234352 0.00126
NM_000458.4(HNF1B):c.*691A>G rs751817675 0.00064
NM_000458.4(HNF1B):c.*629C>T rs566057658 0.00026
NM_000458.4(HNF1B):c.1207-18T>C rs199849203 0.00026
NM_000458.4(HNF1B):c.852C>T (p.His284=) rs149581999 0.00022
NM_000458.4(HNF1B):c.1668C>A (p.Ala556=) rs144354798 0.00019
NC_000017.11:g.37745116G>A rs142612536 0.00015
NM_000458.4(HNF1B):c.*701G>A rs886052888 0.00015
NM_000458.4(HNF1B):c.73G>T (p.Val25Leu) rs139107479 0.00015
NM_000458.4(HNF1B):c.1046-12G>A rs201751705 0.00014
NM_000458.4(HNF1B):c.-82G>T rs886052892 0.00013
NM_000458.4(HNF1B):c.420C>T (p.Val140=) rs370134885 0.00011
NM_000458.4(HNF1B):c.1534+11G>A rs373875820 0.00009
NM_000458.4(HNF1B):c.1578C>G (p.Ser526=) rs751225159 0.00009
NM_000458.4(HNF1B):c.1534+10C>T rs368168569 0.00007
NM_000458.4(HNF1B):c.1339+17G>A rs374854968 0.00006
NM_000458.4(HNF1B):c.36C>T (p.Leu12=) rs749370057 0.00006
NM_000458.4(HNF1B):c.1239C>T (p.Val413=) rs201113814 0.00005
NM_000458.4(HNF1B):c.1654-4G>A rs193922485 0.00005
NM_000458.4(HNF1B):c.1008C>T (p.His336=) rs150268130 0.00004
NM_000458.4(HNF1B):c.1539C>T (p.Tyr513=) rs780554506 0.00004
NM_000458.4(HNF1B):c.*88A>G rs762266343 0.00003
NM_000458.4(HNF1B):c.100C>T (p.Leu34=) rs373201245 0.00003
NM_000458.4(HNF1B):c.1373T>G (p.Val458Gly) rs375644184 0.00002
NM_000458.4(HNF1B):c.314A>G (p.Glu105Gly) rs375625110 0.00002
NM_000458.4(HNF1B):c.*789T>C rs886052887 0.00001
NM_000458.4(HNF1B):c.1025C>T (p.Ser342Phe) rs780035561 0.00001
NM_000458.4(HNF1B):c.1414G>A (p.Val472Ile) rs762841746 0.00001
NM_000458.4(HNF1B):c.66C>A (p.Thr22=) rs906719754 0.00001
NM_000458.4(HNF1B):c.810-17C>T rs759382717 0.00001
NM_000458.4(HNF1B):c.96G>A (p.Glu32=) rs778229703 0.00001
NM_000458.4(HNF1B):c.974G>A (p.Ser325Asn) rs794727624 0.00001
NM_000458.4(HNF1B):c.*37G>A rs1555818071
NM_000458.4(HNF1B):c.1006C>A (p.His336Asn) rs138986885
NM_000458.4(HNF1B):c.1116C>T (p.Ser372=) rs775094591
NM_000458.4(HNF1B):c.1152C>A (p.Val384=)
NM_000458.4(HNF1B):c.1188C>T (p.Leu396=)
NM_000458.4(HNF1B):c.1206+42_1206+46del rs142240844
NM_000458.4(HNF1B):c.1338A>G (p.Gln446=) rs776536485
NM_000458.4(HNF1B):c.1339+12T>C rs1375568430
NM_000458.4(HNF1B):c.1389C>T (p.Ala463=) rs761684626
NM_000458.4(HNF1B):c.1396C>G (p.Leu466Val) rs1555821665
NM_000458.4(HNF1B):c.1418A>G (p.Gln473Arg) rs886052891
NM_000458.4(HNF1B):c.1474G>A (p.Gly492Ser)
NM_000458.4(HNF1B):c.1505C>A (p.Ala502Glu) rs2032548578
NM_000458.4(HNF1B):c.150T>G (p.Pro50=) rs2034119944
NM_000458.4(HNF1B):c.1614C>T (p.Ser538=) rs1568636744
NM_000458.4(HNF1B):c.165G>A (p.Glu55=)
NM_000458.4(HNF1B):c.182T>G (p.Val61Gly)
NM_000458.4(HNF1B):c.226G>T (p.Gly76Cys)
NM_000458.4(HNF1B):c.244G>A (p.Asp82Asn)
NM_000458.4(HNF1B):c.300C>G (p.Thr100=)
NM_000458.4(HNF1B):c.300C>T (p.Thr100=) rs369134247
NM_000458.4(HNF1B):c.309G>C (p.Ala103=) rs1197263675
NM_000458.4(HNF1B):c.375C>A (p.Ile125=)
NM_000458.4(HNF1B):c.402C>T (p.Ile134=) rs1555831433
NM_000458.4(HNF1B):c.429C>T (p.Thr143=)
NM_000458.4(HNF1B):c.438C>T (p.Asn146=) rs2033930573
NM_000458.4(HNF1B):c.544+14T>A rs759120365
NM_000458.4(HNF1B):c.60G>A (p.Gly20=)
NM_000458.4(HNF1B):c.810-4C>G
NM_000458.4(HNF1B):c.819T>C (p.Cys273=) rs1568664272
NM_000458.4(HNF1B):c.831G>A (p.Gly277=) rs199797518
NM_000458.4(HNF1B):c.936G>A (p.Lys312=)
NM_000458.4(HNF1B):c.999C>T (p.Gly333=)
NM_000458.4(HNF1B):c.9C>G (p.Ser3=)

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