List of variants in gene KLHL3 reported as likely benign for autosomal dominant pseudohypoaldosteronism type 1

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 26

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HGVS	dbSNP	gnomAD frequency
NM_017415.3(KLHL3):c.*1451A>G	rs149596381	0.00913
NM_017415.3(KLHL3):c.*1896T>G	rs75344015	0.00578
NM_017415.3(KLHL3):c.*1106G>T	rs141393967	0.00223
NM_017415.3(KLHL3):c.-303G>C	rs567542768	0.00216
NM_017415.3(KLHL3):c.*2267T>A	rs140696146	0.00215
NM_017415.3(KLHL3):c.*3128C>G	rs147801381	0.00197
NM_017415.3(KLHL3):c.*4065C>T	rs142781557	0.00196
NM_017415.3(KLHL3):c.-256T>A	rs182320171	0.00140
NM_017415.3(KLHL3):c.838C>T (p.Leu280=)	rs138650966	0.00095
NM_017415.3(KLHL3):c.*108G>A	rs147305829	0.00076
NM_017415.3(KLHL3):c.*2360G>A	rs533076689	0.00044
NM_017415.3(KLHL3):c.-275G>C	rs189053795	0.00035
NM_017415.3(KLHL3):c.*4006C>T	rs150624383	0.00029
NM_017415.3(KLHL3):c.*2248C>T	rs3813317	0.00019
NM_017415.3(KLHL3):c.*224G>T	rs536807069	0.00019
NM_017415.3(KLHL3):c.904-5C>T	rs375172469	0.00019
NM_017415.3(KLHL3):c.1401C>A (p.Thr467=)	rs35420153	0.00016
NM_017415.3(KLHL3):c.*4066C>T	rs544519958	0.00015
NM_017415.3(KLHL3):c.*2485T>G	rs573842978	0.00014
NM_017415.3(KLHL3):c.1321+10C>T	rs145091610	0.00014
NM_017415.3(KLHL3):c.*299G>A	rs539132895	0.00011
NM_017415.3(KLHL3):c.*2687C>T	rs186283051	0.00010
NM_017415.3(KLHL3):c.*1651C>T	rs577834025	0.00002
NM_017415.3(KLHL3):c.1021+5G>A	rs183499982	0.00002
NM_017415.3(KLHL3):c.*2805A>G	rs141261117	0.00001
NM_017415.3(KLHL3):c.1518C>T (p.Ser506=)	rs529937913	0.00001

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