ClinVar Miner

List of variants in gene WNK1 reported as likely benign for Hereditary sensory and autonomic neuropathy type IIA; Pseudohypoaldosteronism type 2C

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 42
Download table as spreadsheet
HGVS dbSNP
NM_018979.4(WNK1):c.1074C>T (p.Thr358=) rs72648621
NM_018979.4(WNK1):c.108G>C (p.Gly36=) rs375485682
NM_018979.4(WNK1):c.1401-7T>C rs764009301
NM_018979.4(WNK1):c.1536A>G (p.Leu512=) rs1555131208
NM_018979.4(WNK1):c.1689A>G (p.Ser563=) rs1555132915
NM_018979.4(WNK1):c.1834G>A (p.Gly612Ser) rs146450828
NM_018979.4(WNK1):c.1881A>T (p.Val627=) rs748687867
NM_018979.4(WNK1):c.1899G>A (p.Glu633=) rs1555133438
NM_018979.4(WNK1):c.192C>T (p.Asp64=) rs756914631
NM_018979.4(WNK1):c.210G>A (p.Ala70=) rs145076179
NM_018979.4(WNK1):c.2652G>A (p.Ala884=) rs142528714
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.3081C>T (p.Pro1027=) rs150212942
NM_018979.4(WNK1):c.3112-10C>T rs72650715
NM_018979.4(WNK1):c.3387A>C (p.Gly1129=) rs1555148183
NM_018979.4(WNK1):c.3490-4A>G rs143557702
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.3597A>G (p.Glu1199=) rs777111973
NM_018979.4(WNK1):c.3699G>A (p.Ala1233=) rs147752204
NM_018979.4(WNK1):c.3948A>C (p.Thr1316=) rs1201537831
NM_018979.4(WNK1):c.4287G>A (p.Pro1429=) rs1420978472
NM_018979.4(WNK1):c.4320C>T (p.Ile1440=) rs72650730
NM_018979.4(WNK1):c.4563C>T (p.Thr1521=) rs749432947
NM_018979.4(WNK1):c.4564G>A (p.Val1522Met) rs146861951
NM_018979.4(WNK1):c.4635T>C (p.Ser1545=) rs1194260196
NM_018979.4(WNK1):c.5418A>G (p.Pro1806=) rs56245971
NM_018979.4(WNK1):c.6036T>G (p.Ser2012=) rs750142502
NM_018979.4(WNK1):c.6123T>A (p.Leu2041=) rs189148252
NM_018979.4(WNK1):c.6135T>C (p.Asn2045=) rs1555158255
NM_018979.4(WNK1):c.6150T>C (p.Leu2050=) rs151331381
NM_018979.4(WNK1):c.6315G>C (p.Leu2105=) rs376551765
NM_018979.4(WNK1):c.677A>T (p.Glu226Val) rs72647373
NM_018979.4(WNK1):c.6832-8G>A rs772178712
NM_018979.4(WNK1):c.6930T>C (p.Ala2310=) rs1555164326
NM_018979.4(WNK1):c.7119C>T (p.Asn2373=) rs201636547
NM_018979.4(WNK1):c.763C>A (p.Arg255=) rs764593537
NM_018979.4(WNK1):c.774A>G (p.Thr258=) rs1555105614
NM_018979.4(WNK1):c.885G>A (p.Lys295=) rs765502315
NM_018979.4(WNK1):c.915G>A (p.Thr305=) rs72648609
NM_018979.4(WNK1):c.932+7T>A rs371166762

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.