ClinVar Miner

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

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Total variants: 78
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HGVS dbSNP
NM_018979.4(WNK1):c.*1056C>A rs765836409
NM_018979.4(WNK1):c.*1169G>A rs549160638
NM_018979.4(WNK1):c.*1304C>T rs766319091
NM_018979.4(WNK1):c.*1307G>A rs547941922
NM_018979.4(WNK1):c.*1342G>A rs77954451
NM_018979.4(WNK1):c.*143C>A
NM_018979.4(WNK1):c.*148T>C
NM_018979.4(WNK1):c.*164G>A rs767710474
NM_018979.4(WNK1):c.*1678C>G
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.*176C>T
NM_018979.4(WNK1):c.*1869A>G rs886048821
NM_018979.4(WNK1):c.*1971G>C rs536971299
NM_018979.4(WNK1):c.*1982C>T
NM_018979.4(WNK1):c.*1990G>A rs886048825
NM_018979.4(WNK1):c.*2090T>C rs886048826
NM_018979.4(WNK1):c.*2134G>C
NM_018979.4(WNK1):c.*290A>C
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.*533G>C
NM_018979.4(WNK1):c.*558G>C
NM_018979.4(WNK1):c.*613T>C
NM_018979.4(WNK1):c.*642G>A rs886048810
NM_018979.4(WNK1):c.*643G>A rs886048811
NM_018979.4(WNK1):c.*701T>C
NM_018979.4(WNK1):c.*766G>A rs886048814
NM_018979.4(WNK1):c.-234T>C rs368645018
NM_018979.4(WNK1):c.-253A>G rs549380671
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.-368G>T rs886049859
NM_018979.4(WNK1):c.-373G>C
NM_018979.4(WNK1):c.-638C>T
NM_018979.4(WNK1):c.126G>A (p.Ala42=)
NM_018979.4(WNK1):c.145G>A (p.Gly49Ser)
NM_018979.4(WNK1):c.1790G>A (p.Ser597Asn) rs757732497
NM_018979.4(WNK1):c.198T>C (p.Arg66=)
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.2465C>T (p.Ala822Val)
NM_018979.4(WNK1):c.2508C>T (p.Leu836=) rs886049906
NM_018979.4(WNK1):c.2625G>A (p.Thr875=)
NM_018979.4(WNK1):c.264C>T (p.Ser88=) rs773586473
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.3354A>C (p.Pro1118=) rs549781052
NM_018979.4(WNK1):c.3468C>G (p.Pro1156=)
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.3986C>G (p.Thr1329Arg)
NM_018979.4(WNK1):c.4043C>T (p.Thr1348Ile) rs746601991
NM_018979.4(WNK1):c.4091A>G (p.Asn1364Ser)
NM_018979.4(WNK1):c.4490C>T (p.Ser1497Leu)
NM_018979.4(WNK1):c.473G>C (p.Ser158Thr)
NM_018979.4(WNK1):c.4830G>A (p.Val1610=)
NM_018979.4(WNK1):c.4855C>A (p.His1619Asn)
NM_018979.4(WNK1):c.491G>T (p.Arg164Leu) rs886049867
NM_018979.4(WNK1):c.5041T>C (p.Ser1681Pro)
NM_018979.4(WNK1):c.5068C>G (p.Pro1690Ala) rs771546256
NM_018979.4(WNK1):c.5294G>C (p.Gly1765Ala)
NM_018979.4(WNK1):c.5555C>G (p.Ala1852Gly) rs886048785
NM_018979.4(WNK1):c.5878G>T (p.Val1960Leu)
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.7008A>G (p.Gln2336=) rs369782445
NM_018979.4(WNK1):c.7139G>A (p.Arg2380Gln) rs531919850
NM_018979.4(WNK1):c.99C>T (p.Ser33=) rs748052079

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