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

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_017415.3(KLHL3):c.471A>G (p.Ala157=)	rs2905608	0.78307
NM_017415.3(KLHL3):c.*3068A>G	rs3813314	0.65518
NM_017415.3(KLHL3):c.*4210A>G	rs6863414	0.65359
NM_017415.3(KLHL3):c.*2926T>C	rs3813315	0.43732
NM_017415.3(KLHL3):c.*1310C>T	rs2057680	0.43675
NM_017415.3(KLHL3):c.*2080A>C	rs3813318	0.18814
NM_017415.3(KLHL3):c.1383G>A (p.Glu461=)	rs2301708	0.17239
NM_017415.3(KLHL3):c.*1104G>A	rs7444370	0.10673
NM_017415.3(KLHL3):c.*3205A>T	rs35251512	0.09053
NM_017415.3(KLHL3):c.*2404C>A	rs3813316	0.05943
NM_017415.3(KLHL3):c.1611G>T (p.Gly537=)	rs17171525	0.03678
NM_017415.3(KLHL3):c.*3338del	rs58917494

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