List of variants in gene combination ANK2, LOC126807136 reported as benign 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001148.6(ANK2):c.6168C>G (p.Leu2056=)	rs3796928	0.11246
NM_001148.6(ANK2):c.5469C>T (p.Pro1823=)	rs33966911	0.07670
NM_001148.6(ANK2):c.5985G>A (p.Lys1995=)	rs116652427	0.00095
NM_001148.6(ANK2):c.5509G>A (p.Ala1837Thr)	rs199527708	0.00024
NM_001148.6(ANK2):c.5313G>A (p.Lys1771=)	rs140992864	0.00009
NM_001148.6(ANK2):c.5715G>A (p.Ser1905=)	rs143404578	0.00002

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