List of variants in gene combination AKAP9, LOC129998788 reported as uncertain significance for long QT syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_005751.5(AKAP9):c.41A>C (p.Lys14Thr)	rs138107415	0.00058
NM_005751.5(AKAP9):c.48+5G>A	rs377559019	0.00002
NM_005751.5(AKAP9):c.34G>A (p.Ala12Thr)	rs1431417772	0.00001
NM_005751.5(AKAP9):c.15G>T (p.Glu5Asp)
NM_005751.5(AKAP9):c.17G>A (p.Arg6Lys)
NM_005751.5(AKAP9):c.29T>C (p.Leu10Pro)	rs2130422781
NM_005751.5(AKAP9):c.32A>G (p.Glu11Gly)	rs2130422799
NM_005751.5(AKAP9):c.39C>T (p.Gly13=)	rs1376652098
NM_005751.5(AKAP9):c.44C>T (p.Ala15Val)

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