List of variants in gene KLHL9 reported as benign for not provided

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_018847.4(KLHL9):c.1605A>G (p.Gln535=)	rs41270133	0.02825
NM_018847.4(KLHL9):c.1833A>G (p.Ser611=)	rs114638498	0.00719
NM_018847.4(KLHL9):c.992C>T (p.Ala331Val)	rs76705600	0.00238
NM_018847.4(KLHL9):c.1412A>G (p.Asp471Gly)	rs77402394	0.00036
NM_018847.4(KLHL9):c.1830T>C (p.Leu610=)	rs146829226	0.00019
NM_018847.4(KLHL9):c.531C>T (p.Ile177=)	rs541441825	0.00001
NM_018847.4(KLHL9):c.1140G>A (p.Met380Ile)
NM_018847.4(KLHL9):c.51G>A (p.Gln17=)	rs549815739

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