List of variants in gene combination AKAP9, LOC129998789 reported as uncertain significance for long QT syndrome

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_005751.5(AKAP9):c.752T>G (p.Leu251Arg)	rs748330070	0.00003
NM_005751.5(AKAP9):c.793C>G (p.Gln265Glu)	rs1798307146	0.00001
NM_005751.5(AKAP9):c.733-12_733-9del	rs771403705
NM_005751.5(AKAP9):c.740C>G (p.Ala247Gly)
NM_005751.5(AKAP9):c.802C>G (p.Gln268Glu)

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