ClinVar Miner

List of variants in gene WNK1 reported as uncertain significance for Pseudohypoaldosteronism, type 2

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Total variants: 63
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HGVS dbSNP
NM_018979.4(WNK1):c.*1056C>A rs765836409
NM_018979.4(WNK1):c.*1132_*1133del rs546217405
NM_018979.4(WNK1):c.*1304C>T rs766319091
NM_018979.4(WNK1):c.*1342G>A rs77954451
NM_018979.4(WNK1):c.*1347del rs886048817
NM_018979.4(WNK1):c.*164G>A rs767710474
NM_018979.4(WNK1):c.*1690T>C rs886048818
NM_018979.4(WNK1):c.*1744C>T rs886048820
NM_018979.4(WNK1):c.*176C>A rs528692788
NM_018979.4(WNK1):c.*1869A>G rs886048821
NM_018979.4(WNK1):c.*1904_*1906CAC[5] rs778502996
NM_018979.4(WNK1):c.*1904dup rs1555165765
NM_018979.4(WNK1):c.*1971G>C rs536971299
NM_018979.4(WNK1):c.*1990G>A rs886048825
NM_018979.4(WNK1):c.*2090T>C rs886048826
NM_018979.4(WNK1):c.*2192_*2196dup rs568163399
NM_018979.4(WNK1):c.*378A>G rs886048804
NM_018979.4(WNK1):c.*389C>T rs886048805
NM_018979.4(WNK1):c.*441C>G rs753439066
NM_018979.4(WNK1):c.*463C>A rs886048806
NM_018979.4(WNK1):c.*628del rs886048808
NM_018979.4(WNK1):c.*628dup rs886048808
NM_018979.4(WNK1):c.*642G>A rs886048810
NM_018979.4(WNK1):c.*643G>A rs886048811
NM_018979.4(WNK1):c.*762_*763CT[1] rs886048813
NM_018979.4(WNK1):c.*766G>A rs886048814
NM_018979.4(WNK1):c.*772_*776del rs886048815
NM_018979.4(WNK1):c.-260G>T rs886049864
NM_018979.4(WNK1):c.-263C>A rs886049863
NM_018979.4(WNK1):c.-291G>A rs886049862
NM_018979.4(WNK1):c.-308G>T rs886049861
NM_018979.4(WNK1):c.-351dup rs886049860
NM_018979.4(WNK1):c.-368G>T rs886049859
NM_018979.4(WNK1):c.108G>C (p.Gly36=) rs375485682
NM_018979.4(WNK1):c.1434C>T (p.Phe478=) rs61736906
NM_018979.4(WNK1):c.1790G>A (p.Ser597Asn) rs757732497
NM_018979.4(WNK1):c.202G>A (p.Ala68Thr) rs886049865
NM_018979.4(WNK1):c.2246C>T (p.Ala749Val) rs886049905
NM_018979.4(WNK1):c.2333A>G (p.Gln778Arg) rs72649879
NM_018979.4(WNK1):c.2508C>T (p.Leu836=) rs886049906
NM_018979.4(WNK1):c.2652G>A (p.Ala884=) rs142528714
NM_018979.4(WNK1):c.266A>G (p.Asn89Ser) rs886049866
NM_018979.4(WNK1):c.295C>T (p.Pro99Ser) rs563691424
NM_018979.4(WNK1):c.2969A>G (p.Tyr990Cys) rs886049923
NM_018979.4(WNK1):c.3175A>G (p.Thr1059Ala) rs886049924
NM_018979.4(WNK1):c.3188C>T (p.Thr1063Ile) rs201379287
NM_018979.4(WNK1):c.3527C>T (p.Ser1176Leu) rs754769050
NM_018979.4(WNK1):c.3662A>G (p.Gln1221Arg) rs886049925
NM_018979.4(WNK1):c.3845-14G>A rs368270119
NM_018979.4(WNK1):c.3899C>T (p.Ser1300Phe) rs143361850
NM_018979.4(WNK1):c.4270A>G (p.Ile1424Val) rs752331641
NM_018979.4(WNK1):c.4384G>C (p.Gly1462Arg) rs368621387
NM_018979.4(WNK1):c.491G>T (p.Arg164Leu) rs886049867
NM_018979.4(WNK1):c.5258A>G (p.Lys1753Arg) rs752078094
NM_018979.4(WNK1):c.5370G>T (p.Gln1790His) rs773797682
NM_018979.4(WNK1):c.5555C>G (p.Ala1852Gly) rs886048785
NM_018979.4(WNK1):c.5869C>T (p.Arg1957Cys) rs201766777
NM_018979.4(WNK1):c.5943T>G (p.Phe1981Leu) rs72650765
NM_018979.4(WNK1):c.6101A>G (p.His2034Arg) rs72650766
NM_018979.4(WNK1):c.6442C>G (p.Leu2148Val) rs886048786
NM_018979.4(WNK1):c.6825T>C (p.Asn2275=) rs374193324
NM_018979.4(WNK1):c.7139G>A (p.Arg2380Gln) rs531919850
NM_018979.4(WNK1):c.99C>T (p.Ser33=) rs748052079

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