List of variants reported as likely benign for Pseudohypoaldosteronism type 2C

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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_018979.4(WNK1):c.-514C>T	rs577916238	0.00191
NM_018979.4(WNK1):c.446C>T (p.Ala149Val)	rs34880640	0.00091
NM_018979.4(WNK1):c.210G>A (p.Ala70=)	rs145076179	0.00011
NM_018979.4(WNK1):c.*24A>G	rs367692602	0.00009
NM_018979.4(WNK1):c.1434C>T (p.Phe478=)	rs61736906	0.00009
NM_018979.4(WNK1):c.5189C>T (p.Thr1730Ile)	rs375562377	0.00009
NM_018979.4(WNK1):c.108G>C (p.Gly36=)	rs375485682	0.00004
NM_018979.4(WNK1):c.296C>T (p.Pro99Leu)	rs560595238	0.00003
NM_018979.4(WNK1):c.7119C>T (p.Asn2373=)	rs201636547	0.00003
NM_018979.4(WNK1):c.128C>G (p.Ala43Gly)	rs775564750	0.00002
NM_018979.4(WNK1):c.209C>G (p.Ala70Gly)	rs368280492	0.00002
NM_018979.4(WNK1):c.2710A>G (p.Thr904Ala)	rs752492830	0.00001
NM_018979.4(WNK1):c.2926C>T (p.Leu976=)	rs761135188	0.00001
NM_018979.4(WNK1):c.4384G>C (p.Gly1462Arg)	rs368621387	0.00001
NM_018979.4(WNK1):c.5258A>G (p.Lys1753Arg)	rs752078094	0.00001
NM_018979.4(WNK1):c.3845-14G>A	rs368270119

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