List of variants in gene KLHL41 reported by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_006063.3(KLHL41):c.863T>G (p.Leu288Arg)	rs139415849	0.00597
NM_006063.3(KLHL41):c.684A>C (p.Thr228=)	rs141395388	0.00123
NM_006063.3(KLHL41):c.398G>A (p.Gly133Asp)	rs147294651	0.00105
NM_006063.3(KLHL41):c.1569T>C (p.Asp523=)	rs373954289	0.00034
NM_006063.3(KLHL41):c.783C>T (p.Gly261=)	rs141574405	0.00034
NM_006063.3(KLHL41):c.1512T>G (p.Thr504=)	rs1684148189	0.00001
NM_006063.3(KLHL41):c.534A>G (p.Glu178=)	rs769507643	0.00001
NM_006063.3(KLHL41):c.282C>T (p.Ala94=)	rs1684005972
NM_006063.3(KLHL41):c.453C>A (p.Ala151=)

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