ClinVar Miner

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

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Total variants: 24
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HGVS dbSNP
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.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.2374-181C>T rs880054
NM_018979.4(WNK1):c.2490G>A (p.Pro830=) rs79816263
NM_018979.4(WNK1):c.3490-5T>A rs72650719
NM_018979.4(WNK1):c.3654A>G (p.Ser1218=) rs141971833
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.4605_4607del (p.Ser1536del) rs72650732
NM_018979.4(WNK1):c.4983T>C (p.Ser1661=) rs149852592
NM_018979.4(WNK1):c.5281-4G>A rs72650740
NM_018979.4(WNK1):c.5284C>T (p.Leu1762=) rs72650741
NM_018979.4(WNK1):c.5397A>G (p.Gln1799=) rs148639270
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.5496G>A (p.Gln1832=) rs138219481
NM_018979.4(WNK1):c.5542_5550del (p.Thr1848_Ser1850del) rs544395150
NM_018979.4(WNK1):c.5991G>A (p.Glu1997=) rs61736907
NM_018979.4(WNK1):c.684C>T (p.Gly228=) rs72647374

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