ClinVar Miner

List of variants in gene WNK1 reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 94
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HGVS dbSNP gnomAD frequency
NM_018979.4(WNK1):c.6643+136G>A rs56168957 0.01953
NM_018979.4(WNK1):c.5583+233C>T rs66669321 0.01436
NM_018979.4(WNK1):c.5510-191G>A rs79555599 0.00920
NM_018979.4(WNK1):c.*50A>G rs1292018946 0.00906
NM_018979.4(WNK1):c.*277A>T rs80258895 0.00882
NM_018979.4(WNK1):c.5468C>T (p.Pro1823Leu) rs17755373 0.00870
NM_018979.4(WNK1):c.1621-200C>T rs140918667 0.00863
NM_018979.4(WNK1):c.-328C>G rs189463195 0.00854
NM_018979.4(WNK1):c.3844+42G>T rs72650727 0.00835
NM_018979.4(WNK1):c.6643+79G>C rs72650770 0.00835
NM_018979.4(WNK1):c.6246-52C>T rs12305212 0.00817
NM_018979.4(WNK1):c.6246-276A>G rs12307778 0.00816
NM_018979.4(WNK1):c.5991G>A (p.Glu1997=) rs61736907 0.00815
NM_018979.4(WNK1):c.5583+283G>A rs72650760 0.00804
NM_018979.4(WNK1):c.2020A>G (p.Thr674Ala) rs11833299 0.00803
NM_018979.4(WNK1):c.3722-25C>T rs72650726 0.00787
NM_018979.4(WNK1):c.-25C>G rs72647367 0.00762
NM_018979.4(WNK1):c.684C>T (p.Gly228=) rs72647374 0.00748
NM_018979.4(WNK1):c.5481A>G (p.Thr1827=) rs61736908 0.00679
NM_018979.4(WNK1):c.5510-307A>G rs115570118 0.00641
NM_018979.4(WNK1):c.2139+3331G>A rs66780864 0.00636
NM_018979.4(WNK1):c.6245+197_6245+208del rs1168336862 0.00525
NM_018979.4(WNK1):c.6832-22C>T rs56133817 0.00524
NM_018979.4(WNK1):c.6245+199_6245+207del rs1250407490 0.00518
NM_018979.4(WNK1):c.5509+166G>A rs72650754 0.00492
NM_018979.4(WNK1):c.1621-231C>T rs74555557 0.00451
NM_213655.5(WNK1):c.2155A>G (p.Ser719Gly) rs72649807 0.00451
NM_018979.4(WNK1):c.6245+197_6245+198insG rs1380874444 0.00445
NM_018979.4(WNK1):c.2052A>G (p.Ala684=) rs72648690 0.00413
NM_018979.4(WNK1):c.1401-149C>T rs11064572 0.00390
NM_018979.4(WNK1):c.1620+105T>C rs11064574 0.00387
NM_018979.4(WNK1):c.5448+183T>G rs12304405 0.00386
NM_018979.4(WNK1):c.2223+273G>T rs72649877 0.00344
NM_018979.4(WNK1):c.3654A>G (p.Ser1218=) rs141971833 0.00316
NM_018979.4(WNK1):c.5583+3A>G rs72650758 0.00270
NM_018979.4(WNK1):c.5281-4G>A rs72650740 0.00269
NM_213655.5(WNK1):c.2172T>C (p.Val724=) rs72649808 0.00266
NM_213655.5(WNK1):c.2270C>T (p.Pro757Leu) rs562247853 0.00263
NM_018979.4(WNK1):c.5281-271G>A rs193231716 0.00221
NM_018979.4(WNK1):c.2490G>A (p.Pro830=) rs79816263 0.00211
NM_213655.5(WNK1):c.2362C>T (p.Arg788Cys) rs72649848 0.00173
NM_213655.5(WNK1):c.2659T>C (p.Leu887=) rs72649855 0.00167
NM_018979.4(WNK1):c.1074C>T (p.Thr358=) rs72648621 0.00160
NM_018979.4(WNK1):c.6150T>C (p.Leu2050=) rs151331381 0.00157
NM_018979.4(WNK1):c.5284C>T (p.Leu1762=) rs72650741 0.00116
NM_018979.4(WNK1):c.3112-10C>T rs72650715 0.00103
NM_018979.4(WNK1):c.6643+18A>G rs72650769 0.00103
NM_018979.4(WNK1):c.2206A>G (p.Ile736Val) rs147099510 0.00096
NM_018979.4(WNK1):c.1855A>G (p.Thr619Ala) rs149388376 0.00086
NM_018979.4(WNK1):c.1621-29A>G rs74744302 0.00081
NM_018979.4(WNK1):c.3112-30C>T rs149557151 0.00074
NM_018979.4(WNK1):c.4983T>C (p.Ser1661=) rs149852592 0.00072
NM_018979.4(WNK1):c.7021G>A (p.Gly2341Ser) rs146042595 0.00062
NM_018979.4(WNK1):c.4354A>G (p.Thr1452Ala) rs142543401 0.00061
NM_018979.4(WNK1):c.4320C>T (p.Ile1440=) rs72650730 0.00055
NM_018979.4(WNK1):c.915G>A (p.Thr305=) rs72648609 0.00048
NM_018979.4(WNK1):c.6448+38A>G rs181086146 0.00036
NM_213655.5(WNK1):c.2939G>T (p.Ser980Ile) rs372091476 0.00026
NM_213655.5(WNK1):c.2772A>G (p.Glu924=) rs371538921 0.00016
NM_018979.4(WNK1):c.1044C>T (p.Arg348=) rs201400797 0.00014
NM_018979.4(WNK1):c.210G>A (p.Ala70=) rs145076179 0.00011
NM_018979.4(WNK1):c.5418A>G (p.Pro1806=) rs56245971 0.00009
NM_018979.4(WNK1):c.2652G>A (p.Ala884=) rs142528714 0.00006
NM_018979.4(WNK1):c.6030G>A (p.Pro2010=) rs777053734 0.00004
NM_018979.4(WNK1):c.3906T>C (p.Ser1302=) rs1318518629 0.00002
NM_018979.4(WNK1):c.5325C>T (p.Ser1775=) rs373370309 0.00002
NM_018979.4(WNK1):c.261C>T (p.Asp87=) rs1409283366 0.00001
NM_018979.4(WNK1):c.3102A>G (p.Ala1034=) rs747140718 0.00001
NM_018979.4(WNK1):c.6021A>G (p.Leu2007=) rs1466331283 0.00001
NM_018979.4(WNK1):c.1176T>G (p.Pro392=) rs1591900958
NM_018979.4(WNK1):c.1308C>T (p.Thr436=) rs747309501
NM_018979.4(WNK1):c.1620+169_1620+170insGTGTGTGTGTGTGG rs372754842
NM_018979.4(WNK1):c.1620+169_1620+170insGTGTGTGTGTGTGGTT rs369513114
NM_018979.4(WNK1):c.1620+257del rs56249691
NM_018979.4(WNK1):c.1621-75_1621-74del rs11286613
NM_018979.4(WNK1):c.1767C>G (p.Leu589=)
NM_018979.4(WNK1):c.1776G>A (p.Gln592=) rs747700724
NM_018979.4(WNK1):c.2262A>C (p.Thr754=)
NM_018979.4(WNK1):c.2430G>A (p.Ala810=) rs201913428
NM_018979.4(WNK1):c.2463T>C (p.Gly821=) rs760254906
NM_018979.4(WNK1):c.3372+142del rs869267090
NM_018979.4(WNK1):c.4354A>C (p.Thr1452Pro)
NM_018979.4(WNK1):c.447G>C (p.Ala149=) rs753292846
NM_018979.4(WNK1):c.4605_4607del (p.Ser1536del) rs72650732
NM_018979.4(WNK1):c.4968A>G (p.Glu1656=)
NM_018979.4(WNK1):c.5364+236del rs963060376
NM_018979.4(WNK1):c.5542_5550del (p.Thr1848_Ser1850del) rs544395150
NM_018979.4(WNK1):c.6245+155CA[23] rs34202153
NM_018979.4(WNK1):c.6246-36A>T rs55907924
NM_018979.4(WNK1):c.6315G>T (p.Leu2105=) rs376551765
NM_018979.4(WNK1):c.6448+77A>G rs12309420
NM_018979.4(WNK1):c.6831+7C>T rs1462074950
NM_018979.4(WNK1):c.6832-124C>G rs72652207
NM_213655.5(WNK1):c.3201T>C (p.Gly1067=) rs781082488

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