List of variants in gene KCNV2 reported as benign 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
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_133497.4(KCNV2):c.849G>A (p.Glu283=)	rs17656693	0.00801
NM_133497.4(KCNV2):c.1083A>G (p.Gln361=)	rs142744007	0.00709
NM_133497.4(KCNV2):c.762C>G (p.Phe254Leu)	rs147022958

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