ClinVar Miner

List of variants in gene WNK1 reported as likely benign by Illumina Clinical Services Laboratory,Illumina

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Gene type:
ClinVar version:
Total variants: 73
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HGVS dbSNP
NM_018979.4(WNK1):c.*1034T>C rs112549606
NM_018979.4(WNK1):c.*1060C>G rs533399537
NM_018979.4(WNK1):c.*1169G>A rs549160638
NM_018979.4(WNK1):c.*1307G>A rs547941922
NM_018979.4(WNK1):c.*1342G>T rs77954451
NM_018979.4(WNK1):c.*1517T>C rs535956701
NM_018979.4(WNK1):c.*1722_*1725ATTA[1] rs561811313
NM_018979.4(WNK1):c.*1764G>T rs147760490
NM_018979.4(WNK1):c.*1932_*1933AG[1] rs529382173
NM_018979.4(WNK1):c.*1937C>G rs2023943
NM_018979.4(WNK1):c.*277A>T rs80258895
NM_018979.4(WNK1):c.*47C>G rs556130311
NM_018979.4(WNK1):c.*487_*490del rs144238789
NM_018979.4(WNK1):c.*654_*655del rs560549119
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.-213G>T rs372134044
NM_018979.4(WNK1):c.-234T>C rs368645018
NM_018979.4(WNK1):c.-23C>T rs556319875
NM_018979.4(WNK1):c.-253A>G rs549380671
NM_018979.4(WNK1):c.-25C>G rs72647367
NM_018979.4(WNK1):c.-328C>G rs189463195
NM_018979.4(WNK1):c.-598C>G rs544362530
NM_018979.4(WNK1):c.-71G>A rs140209689
NM_018979.4(WNK1):c.1074C>T (p.Thr358=) rs72648621
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.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.2206A>G (p.Ile736Val) rs147099510
NM_018979.4(WNK1):c.2336C>T (p.Ala779Val) rs141428612
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.2624C>G (p.Thr875Arg) rs529032048
NM_018979.4(WNK1):c.2658G>C (p.Pro886=) rs200965163
NM_018979.4(WNK1):c.2895C>T (p.Asn965=) rs138446333
NM_018979.4(WNK1):c.296C>T (p.Pro99Leu) rs560595238
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.3112-10C>T rs72650715
NM_018979.4(WNK1):c.3354A>C (p.Pro1118=) rs549781052
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.3654A>G (p.Ser1218=) rs141971833
NM_018979.4(WNK1):c.3664-15T>A rs201726656
NM_018979.4(WNK1):c.3699G>A (p.Ala1233=) rs147752204
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.4564G>A (p.Val1522Met) rs146861951
NM_018979.4(WNK1):c.4605_4607del (p.Ser1536del) rs567183841
NM_018979.4(WNK1):c.4983T>C (p.Ser1661=) rs149852592
NM_018979.4(WNK1):c.5281-4G>A rs72650740
NM_018979.4(WNK1):c.5481A>G (p.Thr1827=) rs61736908
NM_018979.4(WNK1):c.5496G>A (p.Gln1832=) rs138219481
NM_018979.4(WNK1):c.5574A>T (p.Gly1858=) rs148254159
NM_018979.4(WNK1):c.5583+3A>G rs72650758
NM_018979.4(WNK1):c.5734A>C (p.Ile1912Leu) rs201995891
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.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.6603T>C (p.Asp2201=) rs770912702
NM_018979.4(WNK1):c.684C>T (p.Gly228=) rs72647374
NM_018979.4(WNK1):c.7021G>A (p.Gly2341Ser) rs146042595
NM_018979.4(WNK1):c.915G>A (p.Thr305=) rs72648609

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