ClinVar Miner

List of variants in gene WNK1 reported as benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 144
Download table as spreadsheet
HGVS dbSNP
GRCh37/hg19 12p13.33(chr12:857501-874764)x0
GRCh37/hg19 12p13.33(chr12:863177-874764)x1
GRCh37/hg19 12p13.33(chr12:863517-873411)x1
GRCh37/hg19 12p13.33(chr12:866857-876288)x1
NM_018979.4(WNK1):c.*1034T>C rs112549606
NM_018979.4(WNK1):c.*1145C>T
NM_018979.4(WNK1):c.*1146G>A rs78913352
NM_018979.4(WNK1):c.*1342G>T rs77954451
NM_018979.4(WNK1):c.*1517T>C rs535956701
NM_018979.4(WNK1):c.*1764G>T rs147760490
NM_018979.4(WNK1):c.*1937C>G rs2023943
NM_018979.4(WNK1):c.*1986G>A rs2023944
NM_018979.4(WNK1):c.*2007C>T
NM_018979.4(WNK1):c.*277A>T rs80258895
NM_018979.4(WNK1):c.*409C>T
NM_018979.4(WNK1):c.*47C>G rs556130311
NM_018979.4(WNK1):c.*531C>T
NM_018979.4(WNK1):c.*758C>G rs75767195
NM_018979.4(WNK1):c.-122C>T rs538911254
NM_018979.4(WNK1):c.-159C>T rs72647364
NM_018979.4(WNK1):c.-203C>G rs72647363
NM_018979.4(WNK1):c.-213G>T rs372134044
NM_018979.4(WNK1):c.-23C>T rs556319875
NM_018979.4(WNK1):c.-25C>G rs72647367
NM_018979.4(WNK1):c.-328C>G rs189463195
NM_018979.4(WNK1):c.-34C>T
NM_018979.4(WNK1):c.-452G>A rs118007973
NM_018979.4(WNK1):c.-598C>G rs544362530
NM_018979.4(WNK1):c.-71G>A rs140209689
NM_018979.4(WNK1):c.-91T>G rs3088353
NM_018979.4(WNK1):c.1074C>T (p.Thr358=) rs72648621
NM_018979.4(WNK1):c.1153+40C>G rs2158502
NM_018979.4(WNK1):c.1154-259T>A rs7300056
NM_018979.4(WNK1):c.1287A>G (p.Ala429=) rs10774466
NM_018979.4(WNK1):c.1311+154G>T rs11611246
NM_018979.4(WNK1):c.1312-119G>A rs2240284
NM_018979.4(WNK1):c.1312-203T>C rs2240283
NM_018979.4(WNK1):c.1312-230A>G rs2240282
NM_018979.4(WNK1):c.1401-11C>A rs11064573
NM_018979.4(WNK1):c.1479T>C (p.Asp493=) rs2286006
NM_018979.4(WNK1):c.1512A>G (p.Leu504=) rs56325964
NM_018979.4(WNK1):c.1526T>C (p.Ile509Thr) rs34728563
NM_018979.4(WNK1):c.1834G>A (p.Gly612Ser) rs146450828
NM_018979.4(WNK1):c.1855A>G (p.Thr619Ala) rs149388376
NM_018979.4(WNK1):c.1951+209A>T rs11064575
NM_018979.4(WNK1):c.1994C>T (p.Thr665Ile) rs2286007
NM_018979.4(WNK1):c.2020A>G (p.Thr674Ala) rs11833299
NM_018979.4(WNK1):c.2052A>G (p.Ala684=) rs72648690
NM_018979.4(WNK1):c.2081T>C (p.Ile694Thr) rs61736905
NM_018979.4(WNK1):c.2139+171G>A rs12825084
NM_018979.4(WNK1):c.2139+2855A>G rs72649807
NM_018979.4(WNK1):c.2139+2872T>C rs72649808
NM_018979.4(WNK1):c.2139+2890G>C rs11611231
NM_018979.4(WNK1):c.2139+3014T>C rs193095412
NM_018979.4(WNK1):c.2140-3135T>C rs72649855
NM_018979.4(WNK1):c.2206A>G (p.Ile736Val) rs147099510
NM_018979.4(WNK1):c.2266C>G (p.Gln756Glu) rs768622577
NM_018979.4(WNK1):c.2328G>A (p.Gln776=) rs1012729
NM_018979.4(WNK1):c.2336C>T (p.Ala779Val) rs141428612
NM_018979.4(WNK1):c.2373+20_2373+21dup rs5795952
NM_018979.4(WNK1):c.2373+21dup rs5795952
NM_018979.4(WNK1):c.2374-181C>T rs880054
NM_018979.4(WNK1):c.2401A>G (p.Ile801Val) rs139449198
NM_018979.4(WNK1):c.2468A>G (p.His823Arg) rs56015776
NM_018979.4(WNK1):c.2490G>A (p.Pro830=) rs79816263
NM_018979.4(WNK1):c.2529G>A (p.Gln843=) rs9804992
NM_018979.4(WNK1):c.258T>C (p.Cys86=) rs3168640
NM_018979.4(WNK1):c.2658G>C (p.Pro886=) rs200965163
NM_018979.4(WNK1):c.2664A>G (p.Val888=) rs769020140
NM_018979.4(WNK1):c.2895C>T (p.Asn965=) rs138446333
NM_018979.4(WNK1):c.3016C>T (p.Pro1006Ser) rs186736970
NM_018979.4(WNK1):c.3019A>G (p.Met1007Val) rs191295023
NM_018979.4(WNK1):c.3111+236C>A rs72650711
NM_018979.4(WNK1):c.3112-10C>T rs72650715
NM_018979.4(WNK1):c.3166A>C (p.Thr1056Pro) rs956868
NM_018979.4(WNK1):c.3188C>T (p.Thr1063Ile) rs201379287
NM_018979.4(WNK1):c.3372+273G>A rs113230037
NM_018979.4(WNK1):c.3372+67G>A rs55726687
NM_018979.4(WNK1):c.3489+4C>T rs34032084
NM_018979.4(WNK1):c.3490-5T>A rs72650719
NM_018979.4(WNK1):c.3516A>G (p.Ile1172Met) rs150532648
NM_018979.4(WNK1):c.3578G>A (p.Ser1193Asn) rs72650720
NM_018979.4(WNK1):c.3582G>A (p.Glu1194=) rs72650721
NM_018979.4(WNK1):c.3654A>G (p.Ser1218=) rs141971833
NM_018979.4(WNK1):c.3664-15T>A rs201726656
NM_018979.4(WNK1):c.3698C>T (p.Ala1233Val)
NM_018979.4(WNK1):c.3699G>A (p.Ala1233=) rs147752204
NM_018979.4(WNK1):c.3845-163T>G rs10849576
NM_018979.4(WNK1):c.3859G>T (p.Ala1287Ser) rs149186881
NM_018979.4(WNK1):c.3899C>T (p.Ser1300Phe) rs143361850
NM_018979.4(WNK1):c.3960C>T (p.Asn1320=) rs7300444
NM_018979.4(WNK1):c.4044C>T (p.Thr1348=) rs10849577
NM_018979.4(WNK1):c.421G>A (p.Ala141Thr) rs11554421
NM_018979.4(WNK1):c.4270A>G (p.Ile1424Val) rs752331641
NM_018979.4(WNK1):c.4320C>T (p.Ile1440=) rs72650730
NM_018979.4(WNK1):c.4354A>G (p.Thr1452Ala) rs142543401
NM_018979.4(WNK1):c.446C>T (p.Ala149Val) rs34880640
NM_018979.4(WNK1):c.4517G>C (p.Cys1506Ser) rs7955371
NM_018979.4(WNK1):c.4564G>A (p.Val1522Met) rs146861951
NM_018979.4(WNK1):c.4605_4607del (p.Ser1536del) rs72650732
NM_018979.4(WNK1):c.4983T>C (p.Ser1661=) rs149852592
NM_018979.4(WNK1):c.5280+128A>G rs7975948
NM_018979.4(WNK1):c.5281-182A>T rs12298816
NM_018979.4(WNK1):c.5281-4G>A rs72650740
NM_018979.4(WNK1):c.5284C>T (p.Leu1762=) rs72650741
NM_018979.4(WNK1):c.5364+201G>A rs11064584
NM_018979.4(WNK1):c.5397A>G (p.Gln1799=) rs148639270
NM_018979.4(WNK1):c.5424G>T (p.Met1808Ile) rs12828016
NM_018979.4(WNK1):c.5468C>T (p.Pro1823Leu) rs17755373
NM_018979.4(WNK1):c.5481A>G (p.Thr1827=) rs61736908
NM_018979.4(WNK1):c.5493A>T (p.Thr1831=) rs202024020
NM_018979.4(WNK1):c.5496G>A (p.Gln1832=) rs138219481
NM_018979.4(WNK1):c.5509+83A>G rs2255390
NM_018979.4(WNK1):c.5510-289C>T rs12424810
NM_018979.4(WNK1):c.5513C>T (p.Ser1838Phe)
NM_018979.4(WNK1):c.5542_5550del (p.Thr1848_Ser1850del) rs544395150
NM_018979.4(WNK1):c.5574A>T (p.Gly1858=) rs148254159
NM_018979.4(WNK1):c.5583+177T>C rs2301881
NM_018979.4(WNK1):c.5583+187T>G rs56291311
NM_018979.4(WNK1):c.5583+36C>T rs2301880
NM_018979.4(WNK1):c.5583+3A>G rs72650758
NM_018979.4(WNK1):c.5584-142A>G rs2269937
NM_018979.4(WNK1):c.5601C>T (p.Asp1867=)
NM_018979.4(WNK1):c.578C>A (p.Pro193Gln) rs72647372
NM_018979.4(WNK1):c.5833C>T (p.Arg1945Cys) rs117016551
NM_018979.4(WNK1):c.5851A>G (p.Thr1951Ala) rs72650764
NM_018979.4(WNK1):c.5869C>T (p.Arg1957Cys) rs201766777
NM_018979.4(WNK1):c.5968C>T (p.Pro1990Ser) rs577801497
NM_018979.4(WNK1):c.5991G>A (p.Glu1997=) rs61736907
NM_018979.4(WNK1):c.6032C>A (p.Ser2011Tyr) rs560836712
NM_018979.4(WNK1):c.6150T>C (p.Leu2050=) rs151331381
NM_018979.4(WNK1):c.6449-270G>A rs11611051
NM_018979.4(WNK1):c.6497C>T (p.Thr2166Ile)
NM_018979.4(WNK1):c.6603T>C (p.Asp2201=) rs770912702
NM_018979.4(WNK1):c.6624C>A (p.Ser2208Arg) rs72650768
NM_018979.4(WNK1):c.6828C>T (p.Tyr2276=) rs4766334
NM_018979.4(WNK1):c.684C>T (p.Gly228=) rs72647374
NM_018979.4(WNK1):c.6891G>A (p.Ser2297=) rs201600155
NM_018979.4(WNK1):c.7021G>A (p.Gly2341Ser) rs146042595
NM_018979.4(WNK1):c.759+15A>C rs11064518
NM_018979.4(WNK1):c.759+16_759+18dup rs398088143
NM_018979.4(WNK1):c.759+18_759+19dup rs1565378497
NM_018979.4(WNK1):c.759+27G>A rs3858703
NM_018979.4(WNK1):c.915G>A (p.Thr305=) rs72648609

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.