ClinVar Miner

List of variants in gene WNK1 reported as benign by GeneDx

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Total variants: 33
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HGVS dbSNP
NM_018979.4(WNK1):c.-91T>G rs3088353
NM_018979.4(WNK1):c.1153+40C>G
NM_018979.4(WNK1):c.1154-259T>A
NM_018979.4(WNK1):c.1311+154G>T
NM_018979.4(WNK1):c.1312-119G>A
NM_018979.4(WNK1):c.1312-203T>C
NM_018979.4(WNK1):c.1312-230A>G
NM_018979.4(WNK1):c.1401-11C>A rs11064573
NM_018979.4(WNK1):c.1479T>C (p.Asp493=) rs2286006
NM_018979.4(WNK1):c.1951+209A>T
NM_018979.4(WNK1):c.1994C>T (p.Thr665Ile) rs2286007
NM_018979.4(WNK1):c.2139+171G>A
NM_018979.4(WNK1):c.2139+2890G>C
NM_018979.4(WNK1):c.3111+236C>A
NM_018979.4(WNK1):c.3372+273G>A
NM_018979.4(WNK1):c.3372+67G>A
NM_018979.4(WNK1):c.3845-163T>G
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.5280+128A>G
NM_018979.4(WNK1):c.5281-182A>T
NM_018979.4(WNK1):c.5364+201G>A
NM_018979.4(WNK1):c.5509+83A>G
NM_018979.4(WNK1):c.5510-289C>T
NM_018979.4(WNK1):c.5583+177T>C
NM_018979.4(WNK1):c.5583+187T>G
NM_018979.4(WNK1):c.5583+36C>T
NM_018979.4(WNK1):c.5584-142A>G
NM_018979.4(WNK1):c.6449-270G>A
NM_018979.4(WNK1):c.759+15A>C rs11064518
NM_018979.4(WNK1):c.759+27G>A
NM_213655.4:c.3867+1031C>T

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