ClinVar Miner

List of variants in gene WNK1 reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 109
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_018979.4(WNK1):c.865T>C (p.Ser289Pro) rs200234585 0.00022
NM_213655.5(WNK1):c.2143C>T (p.Arg715Cys) rs772257923 0.00017
NM_018979.4(WNK1):c.3508C>G (p.Leu1170Val) rs142181848 0.00015
NM_018979.4(WNK1):c.4788A>G (p.Gln1596=) rs371448826 0.00012
NM_018979.4(WNK1):c.4487C>G (p.Thr1496Ser) rs763829194 0.00010
NM_018979.4(WNK1):c.4798A>G (p.Ile1600Val) rs975581838 0.00010
NM_213655.5(WNK1):c.2146C>T (p.Arg716Cys) rs140331977 0.00009
NM_018979.4(WNK1):c.3806G>A (p.Arg1269Gln) rs574104473 0.00007
NM_018979.4(WNK1):c.7147T>A (p.Ter2383Lys) rs55650617 0.00007
NM_213655.5(WNK1):c.2351G>A (p.Arg784His) rs769105175 0.00007
NM_018979.4(WNK1):c.4878G>C (p.Leu1626Phe) rs748898332 0.00006
NM_018979.4(WNK1):c.5144A>G (p.Asn1715Ser) rs756614581 0.00006
NM_018979.4(WNK1):c.5870G>A (p.Arg1957His) rs36083875 0.00006
NM_018979.4(WNK1):c.6278G>A (p.Arg2093His) rs200315094 0.00006
NM_213655.5(WNK1):c.2363G>A (p.Arg788His) rs762594801 0.00006
NM_018979.4(WNK1):c.29G>A (p.Ser10Asn) rs867437047 0.00005
NM_018979.4(WNK1):c.7138C>T (p.Arg2380Trp) rs56262445 0.00005
NM_213655.5(WNK1):c.2152C>T (p.Arg718Cys) rs786205473 0.00005
NM_018979.4(WNK1):c.1820C>A (p.Pro607His) rs540823007 0.00004
NM_018979.4(WNK1):c.187A>C (p.Lys63Gln) rs780699781 0.00004
NM_018979.4(WNK1):c.1963G>C (p.Val655Leu) rs370488966 0.00004
NM_018979.4(WNK1):c.4135A>G (p.Thr1379Ala) rs758763241 0.00004
NM_018979.4(WNK1):c.4388G>A (p.Ser1463Asn) rs757201529 0.00004
NM_018979.4(WNK1):c.5998G>C (p.Glu2000Gln) rs774666279 0.00004
NM_018979.4(WNK1):c.6322G>A (p.Val2108Met) rs1437946999 0.00004
NM_213655.5(WNK1):c.2350C>T (p.Arg784Cys) rs758110645 0.00004
NM_213655.5(WNK1):c.2380C>T (p.Leu794Phe) rs773790877 0.00004
NM_213655.5(WNK1):c.3020C>T (p.Pro1007Leu) rs539230381 0.00004
NM_018979.4(WNK1):c.130G>A (p.Ala44Thr) rs764240024 0.00003
NM_018979.4(WNK1):c.1787C>T (p.Ser596Phe) rs144114167 0.00003
NM_018979.4(WNK1):c.2684A>G (p.Gln895Arg) rs200100184 0.00003
NM_018979.4(WNK1):c.5326G>A (p.Glu1776Lys) rs551435012 0.00003
NM_018979.4(WNK1):c.568G>A (p.Ala190Thr) rs1229285578 0.00003
NM_018979.4(WNK1):c.576G>C (p.Glu192Asp) rs971232152 0.00003
NM_213655.5(WNK1):c.2147G>A (p.Arg716His) rs150330647 0.00003
NM_213655.5(WNK1):c.2162C>T (p.Ser721Leu) rs556259173 0.00003
NM_213655.5(WNK1):c.2926G>A (p.Gly976Ser) rs369073199 0.00003
NM_018979.4(WNK1):c.2043T>G (p.His681Gln) rs180681076 0.00002
NM_018979.4(WNK1):c.2105C>A (p.Ser702Tyr) rs772771448 0.00002
NM_018979.4(WNK1):c.4043C>T (p.Thr1348Ile) rs746601991 0.00002
NM_018979.4(WNK1):c.404A>G (p.Gln135Arg) rs750301176 0.00002
NM_018979.4(WNK1):c.413C>T (p.Pro138Leu) rs1277355342 0.00002
NM_018979.4(WNK1):c.4357G>A (p.Val1453Ile) rs774635947 0.00002
NM_018979.4(WNK1):c.4364C>T (p.Ala1455Val) rs759951096 0.00002
NM_018979.4(WNK1):c.4823C>T (p.Ala1608Val) rs781667314 0.00002
NM_018979.4(WNK1):c.4826A>G (p.Asn1609Ser) rs775933163 0.00002
NM_018979.4(WNK1):c.521G>A (p.Ser174Asn) rs1012754203 0.00002
NM_018979.4(WNK1):c.5325C>T (p.Ser1775=) rs373370309 0.00002
NM_018979.4(WNK1):c.6230G>A (p.Arg2077Gln) rs771385000 0.00002
NM_018979.4(WNK1):c.7003G>A (p.Ala2335Thr) rs375901694 0.00002
NM_213655.5(WNK1):c.2233G>A (p.Ala745Thr) rs763686798 0.00002
NM_213655.5(WNK1):c.2359C>T (p.Arg787Ter) rs748504277 0.00002
NM_213655.5(WNK1):c.3218G>A (p.Arg1073His) rs745947901 0.00002
NM_018979.4(WNK1):c.131C>T (p.Ala44Val) rs754447060 0.00001
NM_018979.4(WNK1):c.1606G>C (p.Val536Leu) rs145646194 0.00001
NM_018979.4(WNK1):c.1620+4A>C rs765206647 0.00001
NM_018979.4(WNK1):c.1621-3T>C rs746698174 0.00001
NM_018979.4(WNK1):c.1701G>C (p.Arg567Ser) rs1280224791 0.00001
NM_018979.4(WNK1):c.1823C>G (p.Ser608Cys) rs1455320237 0.00001
NM_018979.4(WNK1):c.2006T>G (p.Val669Gly) rs756433100 0.00001
NM_018979.4(WNK1):c.2625G>A (p.Thr875=) rs763000812 0.00001
NM_018979.4(WNK1):c.2969A>G (p.Tyr990Cys) rs886049923 0.00001
NM_018979.4(WNK1):c.3029T>C (p.Val1010Ala) rs769099133 0.00001
NM_018979.4(WNK1):c.3215A>C (p.His1072Pro) rs376433723 0.00001
NM_018979.4(WNK1):c.3545G>A (p.Arg1182Gln) rs749563110 0.00001
NM_018979.4(WNK1):c.392C>G (p.Ser131Cys) rs763490893 0.00001
NM_018979.4(WNK1):c.418G>A (p.Ala140Thr) rs777744427 0.00001
NM_018979.4(WNK1):c.428C>G (p.Pro143Arg) rs1231436981 0.00001
NM_018979.4(WNK1):c.5057G>A (p.Ser1686Asn) rs773910482 0.00001
NM_018979.4(WNK1):c.5312G>T (p.Gly1771Val) rs770566791 0.00001
NM_018979.4(WNK1):c.5442G>A (p.Ala1814=) rs557930357 0.00001
NM_018979.4(WNK1):c.5530C>T (p.Pro1844Ser) rs769345308 0.00001
NM_018979.4(WNK1):c.5818C>T (p.Pro1940Ser) rs1416374405 0.00001
NM_018979.4(WNK1):c.595C>G (p.Gln199Glu) rs1404174344 0.00001
NM_018979.4(WNK1):c.6110G>A (p.Ser2037Asn) rs1273114507 0.00001
NM_018979.4(WNK1):c.6670G>T (p.Ala2224Ser) rs763836773 0.00001
NM_018979.4(WNK1):c.6797G>T (p.Gly2266Val) rs770327670 0.00001
NM_018979.4(WNK1):c.6986C>T (p.Pro2329Leu) rs781574573 0.00001
NM_018979.4(WNK1):c.7058C>A (p.Pro2353His) rs375566748 0.00001
NM_018979.4(WNK1):c.7092del (p.Ser2365fs) rs1565626117 0.00001
NM_018979.4(WNK1):c.94G>T (p.Asp32Tyr) rs1364175663 0.00001
NM_213655.5(WNK1):c.2245T>C (p.Cys749Arg) rs370768693 0.00001
NM_213655.5(WNK1):c.2291T>C (p.Phe764Ser) rs1218729720 0.00001
NM_213655.5(WNK1):c.2354A>C (p.Lys785Thr) rs1190765461 0.00001
NM_213655.5(WNK1):c.2408C>T (p.Ala803Val) rs774021513 0.00001
NM_213655.5(WNK1):c.2890A>G (p.Met964Val) rs377113516 0.00001
NM_213655.5(WNK1):c.3293G>A (p.Gly1098Asp) rs376606314 0.00001
NM_213655.5(WNK1):c.3415T>C (p.Ser1139Pro) rs748557001 0.00001
NM_018979.4(WNK1):c.1269G>A (p.Ser423=) rs955095527
NM_018979.4(WNK1):c.1476A>T (p.Glu492Asp) rs750205260
NM_018979.4(WNK1):c.2303C>T (p.Ala768Val) rs757239881
NM_018979.4(WNK1):c.2947G>C (p.Glu983Gln) rs1185591309
NM_018979.4(WNK1):c.3326G>A (p.Arg1109His) rs750478389
NM_018979.4(WNK1):c.3372+3A>G rs1426580785
NM_018979.4(WNK1):c.3590G>T (p.Ser1197Ile) rs1592165053
NM_018979.4(WNK1):c.3991C>T (p.Pro1331Ser) rs200513331
NM_018979.4(WNK1):c.4022G>C (p.Ser1341Thr) rs1301534353
NM_018979.4(WNK1):c.464C>A (p.Thr155Asn) rs940919645
NM_018979.4(WNK1):c.5314A>C (p.Thr1772Pro) rs1183977237
NM_018979.4(WNK1):c.5936C>A (p.Pro1979His) rs1954736870
NM_018979.4(WNK1):c.6061A>G (p.Arg2021Gly) rs1954746383
NM_018979.4(WNK1):c.6310A>G (p.Lys2104Glu) rs1310976331
NM_018979.4(WNK1):c.6631G>C (p.Ala2211Pro) rs1955178531
NM_018979.4(WNK1):c.6883A>T (p.Met2295Leu) rs762667877
NM_018979.4(WNK1):c.6923C>T (p.Ala2308Val) rs1955893159
NM_018979.4(WNK1):c.74C>T (p.Pro25Leu) rs1211154368
NM_213655.5(WNK1):c.2328_2344del (p.Pro777fs) rs1371980928
NM_213655.5(WNK1):c.2568C>G (p.His856Gln) rs767616683
NM_213655.5(WNK1):c.2684C>G (p.Thr895Ser) rs370517971

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.