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: 67
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HGVS dbSNP
NM_018979.4(WNK1):c.108G>C (p.Gly36=) rs375485682
NM_018979.4(WNK1):c.1161A>G (p.Pro387=) rs1472444613
NM_018979.4(WNK1):c.1176T>G (p.Pro392=) rs1591900958
NM_018979.4(WNK1):c.1266C>T (p.Tyr422=) rs780974617
NM_018979.4(WNK1):c.1284T>C (p.Ala428=) rs748037310
NM_018979.4(WNK1):c.1308C>T (p.Thr436=) rs747309501
NM_018979.4(WNK1):c.1536A>G (p.Leu512=) rs1555131208
NM_018979.4(WNK1):c.1743A>G (p.Lys581=) rs757328136
NM_018979.4(WNK1):c.1788C>T (p.Ser596=) rs377558862
NM_018979.4(WNK1):c.1827T>A (p.Ala609=) rs1592059818
NM_018979.4(WNK1):c.1881A>T (p.Val627=) rs748687867
NM_018979.4(WNK1):c.1920A>G (p.Leu640=) rs759367944
NM_018979.4(WNK1):c.2139+2872T>C rs72649808
NM_018979.4(WNK1):c.2139+2896G>A rs72649826
NM_018979.4(WNK1):c.2139+2932C>T rs752499633
NM_018979.4(WNK1):c.2139+3331G>A rs66780864
NM_018979.4(WNK1):c.2140-2593T>C rs781082488
NM_018979.4(WNK1):c.237C>T (p.Phe79=) rs931039841
NM_018979.4(WNK1):c.2463T>C (p.Gly821=) rs760254906
NM_018979.4(WNK1):c.2490G>A (p.Pro830=) rs79816263
NM_018979.4(WNK1):c.261C>T (p.Asp87=) rs1409283366
NM_018979.4(WNK1):c.264C>T (p.Ser88=) rs773586473
NM_018979.4(WNK1):c.2664A>G (p.Val888=) rs769020140
NM_018979.4(WNK1):c.2796T>C (p.Ala932=) rs745823883
NM_018979.4(WNK1):c.2926C>T (p.Leu976=) rs761135188
NM_018979.4(WNK1):c.2943G>C (p.Pro981=) rs72650706
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.3102A>G (p.Ala1034=) rs747140718
NM_018979.4(WNK1):c.3210-10A>C rs769825037
NM_018979.4(WNK1):c.33C>T (p.Ser11=) rs776535900
NM_018979.4(WNK1):c.3528G>A (p.Ser1176=) rs150741196
NM_018979.4(WNK1):c.3722-4C>T rs868675360
NM_018979.4(WNK1):c.3930T>A (p.Leu1310=) rs1592171319
NM_018979.4(WNK1):c.3948A>C (p.Thr1316=) rs1201537831
NM_018979.4(WNK1):c.4155A>G (p.Gly1385=) rs1592172276
NM_018979.4(WNK1):c.4194C>T (p.Leu1398=) rs1592172471
NM_018979.4(WNK1):c.4362A>G (p.Ser1454=) rs1592173251
NM_018979.4(WNK1):c.4380A>G (p.Ala1460=) rs200205583
NM_018979.4(WNK1):c.447G>C (p.Ala149=) rs753292846
NM_018979.4(WNK1):c.4575C>T (p.Ser1525=) rs577520430
NM_018979.4(WNK1):c.4578A>G (p.Ala1526=) rs541711074
NM_018979.4(WNK1):c.4605_4607del (p.Ser1536del) rs72650732
NM_018979.4(WNK1):c.4680T>C (p.Tyr1560=) rs1170260349
NM_018979.4(WNK1):c.4941T>C (p.Pro1647=) rs1592176190
NM_018979.4(WNK1):c.5043A>T (p.Ser1681=) rs1592176549
NM_018979.4(WNK1):c.5088T>G (p.Ala1696=) rs1465426918
NM_018979.4(WNK1):c.5409A>G (p.Thr1803=) rs760294868
NM_018979.4(WNK1):c.5502G>A (p.Gln1834=) rs751308963
NM_018979.4(WNK1):c.5509+166G>A rs72650754
NM_018979.4(WNK1):c.5510-7_5510-4del rs1592219606
NM_018979.4(WNK1):c.5968C>T (p.Pro1990Ser) rs577801497
NM_018979.4(WNK1):c.60G>A (p.Pro20=) rs72647368
NM_018979.4(WNK1):c.6123T>C (p.Leu2041=) rs189148252
NM_018979.4(WNK1):c.6135T>C (p.Asn2045=) rs1555158255
NM_018979.4(WNK1):c.6183C>T (p.Ser2061=) rs201207378
NM_018979.4(WNK1):c.6201C>T (p.Ile2067=) rs748760769
NM_018979.4(WNK1):c.6237A>G (p.Leu2079=) rs1321787797
NM_018979.4(WNK1):c.6315G>T (p.Leu2105=) rs376551765
NM_018979.4(WNK1):c.6450T>C (p.Gly2150=) rs747665801
NM_018979.4(WNK1):c.6643+136G>A rs56168957
NM_018979.4(WNK1):c.6738C>T (p.Phe2246=) rs1391656490
NM_018979.4(WNK1):c.6831+6TC[2] rs1372050569
NM_018979.4(WNK1):c.6831+7C>T rs1462074950
NM_018979.4(WNK1):c.6849G>A (p.Arg2283=) rs747605646
NM_018979.4(WNK1):c.7143C>A (p.Thr2381=) rs369472011
NM_018979.4(WNK1):c.93C>T (p.Ser31=) rs372795300

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