ClinVar Miner

List of variants in gene WNK1 studied for Pseudohypoaldosteronism type 2A

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Total variants: 25
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HGVS dbSNP gnomAD frequency
NM_018979.4(WNK1):c.759+16_759+18dup rs398088143 0.08796
NM_018979.4(WNK1):c.*1904dup rs1555165765 0.00019
NM_018979.4(WNK1):c.2652G>A (p.Ala884=) rs142528714 0.00006
NM_018979.4(WNK1):c.5734A>C (p.Ile1912Leu) rs201995891 0.00006
NM_018979.4(WNK1):c.2624C>G (p.Thr875Arg) rs529032048 0.00003
NM_018979.4(WNK1):c.*1060C>G rs533399537 0.00002
NM_018979.4(WNK1):c.*2576_*2579dup rs886048832 0.00001
NM_018979.4(WNK1):c.*1132_*1133del rs546217405
NM_018979.4(WNK1):c.*1347del rs886048817
NM_018979.4(WNK1):c.*1722ATTA[1] rs561811313
NM_018979.4(WNK1):c.*1904CAC[5] rs778502996
NM_018979.4(WNK1):c.*1932AG[1] rs529382173
NM_018979.4(WNK1):c.*2192_*2196dup rs568163399
NM_018979.4(WNK1):c.*2378_*2381dup rs1399161251
NM_018979.4(WNK1):c.*2615_*2618dup rs376351532
NM_018979.4(WNK1):c.*487_*490del rs144238789
NM_018979.4(WNK1):c.*628del rs886048808
NM_018979.4(WNK1):c.*628dup rs886048808
NM_018979.4(WNK1):c.*654_*655del rs560549119
NM_018979.4(WNK1):c.*762CT[1] rs886048813
NM_018979.4(WNK1):c.*772_*776del rs886048815
NM_018979.4(WNK1):c.-308G>T rs886049861
NM_018979.4(WNK1):c.-351dup rs886049860
NM_018979.4(WNK1):c.4605_4607del (p.Ser1536del) rs72650732
NM_018979.4(WNK1):c.5370G>T (p.Gln1790His) rs773797682

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