ClinVar Miner

List of variants in gene WNK1 reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 38
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HGVS dbSNP
GRCh37/hg19 12p13.33(chr12:857501-874764)x0
GRCh37/hg19 12p13.33(chr12:863177-874764)x1
GRCh37/hg19 12p13.33(chr12:863517-873411)x1
GRCh37/hg19 12p13.33(chr12:866857-876288)x1
NM_018979.4(WNK1):c.-91T>G rs3088353
NM_018979.4(WNK1):c.1153+40C>G rs2158502
NM_018979.4(WNK1):c.1154-259T>A rs7300056
NM_018979.4(WNK1):c.1311+154G>T rs11611246
NM_018979.4(WNK1):c.1312-119G>A rs2240284
NM_018979.4(WNK1):c.1312-203T>C rs2240283
NM_018979.4(WNK1):c.1312-230A>G rs2240282
NM_018979.4(WNK1):c.1951+209A>T rs11064575
NM_018979.4(WNK1):c.2139+171G>A rs12825084
NM_018979.4(WNK1):c.2139+2890G>C rs11611231
NM_018979.4(WNK1):c.2373+20_2373+21dup rs5795952
NM_018979.4(WNK1):c.2373+21dup rs5795952
NM_018979.4(WNK1):c.2374-181C>T rs880054
NM_018979.4(WNK1):c.3111+236C>A rs72650711
NM_018979.4(WNK1):c.3372+273G>A rs113230037
NM_018979.4(WNK1):c.3372+67G>A rs55726687
NM_018979.4(WNK1):c.3845-163T>G rs10849576
NM_018979.4(WNK1):c.421G>A (p.Ala141Thr) rs11554421
NM_018979.4(WNK1):c.5280+128A>G rs7975948
NM_018979.4(WNK1):c.5281-182A>T rs12298816
NM_018979.4(WNK1):c.5364+201G>A rs11064584
NM_018979.4(WNK1):c.5468C>T (p.Pro1823Leu) rs17755373
NM_018979.4(WNK1):c.5493A>T (p.Thr1831=) rs202024020
NM_018979.4(WNK1):c.5509+83A>G rs2255390
NM_018979.4(WNK1):c.5510-289C>T rs12424810
NM_018979.4(WNK1):c.5583+177T>C rs2301881
NM_018979.4(WNK1):c.5583+187T>G rs56291311
NM_018979.4(WNK1):c.5583+36C>T rs2301880
NM_018979.4(WNK1):c.5584-142A>G rs2269937
NM_018979.4(WNK1):c.6449-270G>A rs11611051
NM_018979.4(WNK1):c.684C>T (p.Gly228=) rs72647374
NM_018979.4(WNK1):c.759+15A>C rs11064518
NM_018979.4(WNK1):c.759+18_759+19dup rs1565378497
NM_018979.4(WNK1):c.759+27G>A rs3858703

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