List of variants in gene AKAP9 reported as uncertain significance for heart conduction disease

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_005751.5(AKAP9):c.11297G>A (p.Arg3766Gln)	rs137892407	0.00016
NM_005751.5(AKAP9):c.10591C>G (p.Gln3531Glu)	rs767137372	0.00001

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