List of variants in gene KLHL41 reported as benign by PreventionGenetics, part of Exact Sciences

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_006063.3(KLHL41):c.811G>A (p.Ala271Thr)	rs28763868	0.08132
NM_006063.3(KLHL41):c.1251A>G (p.Val417=)	rs79580851	0.01239
NM_006063.3(KLHL41):c.8C>T (p.Ser3Phe)	rs28730867	0.00983
NM_006063.3(KLHL41):c.1441A>G (p.Met481Val)	rs34623017	0.00692
NM_006063.3(KLHL41):c.863T>G (p.Leu288Arg)	rs139415849	0.00597
NM_006063.3(KLHL41):c.15G>A (p.Arg5=)	rs144048872	0.00495
NM_006063.3(KLHL41):c.1737T>C (p.Ala579=)	rs76875207	0.00160
NM_006063.3(KLHL41):c.197T>C (p.Ile66Thr)	rs116809051	0.00138

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