ClinVar Miner

List of variants in gene WNK1 reported as benign for Hereditary sensory and autonomic neuropathy type II

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Total variants: 24
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NM_018979.4(WNK1):c.*1146G>A rs78913352
NM_018979.4(WNK1):c.*1986G>A rs2023944
NM_018979.4(WNK1):c.-203C>G rs72647363
NM_018979.4(WNK1):c.-452G>A rs118007973
NM_018979.4(WNK1):c.-91T>G rs3088353
NM_018979.4(WNK1):c.1287A>G (p.Ala429=) rs10774466
NM_018979.4(WNK1):c.1401-11C>A rs11064573
NM_018979.4(WNK1):c.1479T>C (p.Asp493=) rs2286006
NM_018979.4(WNK1):c.1994C>T (p.Thr665Ile) rs2286007
NM_018979.4(WNK1):c.2328G>A (p.Gln776=) rs1012729
NM_018979.4(WNK1):c.2529G>A (p.Gln843=) rs9804992
NM_018979.4(WNK1):c.258T>C (p.Cys86=) rs3168640
NM_018979.4(WNK1):c.3166A>C (p.Thr1056Pro) rs956868
NM_018979.4(WNK1):c.3489+4C>T rs34032084
NM_018979.4(WNK1):c.3960C>T (p.Asn1320=) rs7300444
NM_018979.4(WNK1):c.4044C>T (p.Thr1348=) rs10849577
NM_018979.4(WNK1):c.421G>A (p.Ala141Thr) rs11554421
NM_018979.4(WNK1):c.4517G>C (p.Cys1506Ser) rs7955371
NM_018979.4(WNK1):c.5397A>G (p.Gln1799=) rs148639270
NM_018979.4(WNK1):c.5424G>T (p.Met1808Ile) rs12828016
NM_018979.4(WNK1):c.5468C>T (p.Pro1823Leu) rs17755373
NM_018979.4(WNK1):c.6828C>T (p.Tyr2276=) rs4766334
NM_018979.4(WNK1):c.759+15A>C rs11064518
NM_018979.4(WNK1):c.759+16_759+18dup rs398088143

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