ClinVar Miner

List of variants in gene WNK1 reported as uncertain significance by GeneDx

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Total variants: 41
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HGVS dbSNP gnomAD frequency
NM_213655.5(WNK1):c.2201C>T (p.Pro734Leu) rs564717613 0.00161
NM_018979.4(WNK1):c.5638G>A (p.Ala1880Thr) rs72650763 0.00097
NM_018979.4(WNK1):c.578C>A (p.Pro193Gln) rs72647372 0.00058
NM_213655.5(WNK1):c.2834G>A (p.Arg945Gln) rs773884230 0.00041
NM_213655.5(WNK1):c.3371G>A (p.Gly1124Glu) rs201042606 0.00024
NM_213655.5(WNK1):c.2533C>T (p.Arg845Cys) rs200794710 0.00011
NM_213655.5(WNK1):c.2605C>A (p.Leu869Ile) rs377073379 0.00011
NM_213655.5(WNK1):c.3107C>T (p.Ala1036Val) rs187534119 0.00009
NM_018979.4(WNK1):c.5734A>C (p.Ile1912Leu) rs201995891 0.00006
NM_018979.4(WNK1):c.6278G>A (p.Arg2093His) rs200315094 0.00006
NM_213655.5(WNK1):c.2833C>T (p.Arg945Trp) rs185749579 0.00006
NM_018979.4(WNK1):c.4265T>G (p.Val1422Gly) rs779654189 0.00004
NM_213655.5(WNK1):c.2650G>A (p.Val884Ile) rs764190549 0.00004
NM_213655.5(WNK1):c.2679A>C (p.Arg893Ser) rs1429843547 0.00003
NM_213655.5(WNK1):c.2831C>T (p.Ala944Val) rs780984459 0.00003
NM_018979.4(WNK1):c.5943T>G (p.Phe1981Leu) rs72650765 0.00002
NM_018979.4(WNK1):c.3215A>C (p.His1072Pro) rs376433723 0.00001
NM_018979.4(WNK1):c.5002T>G (p.Ser1668Ala) rs371813651 0.00001
NM_018979.4(WNK1):c.5258A>G (p.Lys1753Arg) rs752078094 0.00001
NM_213655.5(WNK1):c.2531G>A (p.Arg844Gln) rs765108175 0.00001
NM_213655.5(WNK1):c.2608C>A (p.Leu870Ile) rs762647323 0.00001
NM_213655.5(WNK1):c.3044C>T (p.Ser1015Phe) rs769973198 0.00001
NM_213655.5(WNK1):c.3232C>T (p.Arg1078Trp) rs1383005865 0.00001
NM_213655.5(WNK1):c.3515A>G (p.His1172Arg) rs1064796902 0.00001
NM_018979.4(WNK1):c.1088C>T (p.Ser363Leu) rs1555112931
NM_018979.4(WNK1):c.2840C>A (p.Pro947Gln)
NM_018979.4(WNK1):c.2970C>A (p.Tyr990Ter)
NM_018979.4(WNK1):c.4529G>A (p.Ser1510Asn)
NM_018979.4(WNK1):c.4815G>C (p.Gln1605His)
NM_018979.4(WNK1):c.5489G>A (p.Gly1830Glu)
NM_018979.4(WNK1):c.6624C>A (p.Ser2208Arg) rs72650768
NM_018979.4(WNK1):c.6650G>T (p.Ser2217Ile) rs2154103905
NM_213655.5(WNK1):c.2250dup (p.Ser751fs)
NM_213655.5(WNK1):c.2473C>T (p.Arg825Cys) rs1013040631
NM_213655.5(WNK1):c.2743G>A (p.Asp915Asn)
NM_213655.5(WNK1):c.2869T>C (p.Ser957Pro) rs1379384995
NM_213655.5(WNK1):c.2966A>G (p.Gln989Arg) rs879253973
NM_213655.5(WNK1):c.2990A>G (p.Gln997Arg)
NM_213655.5(WNK1):c.3032T>C (p.Leu1011Pro)
NM_213655.5(WNK1):c.3364C>T (p.Pro1122Ser)
NM_213655.5(WNK1):c.3481C>T (p.Pro1161Ser)

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