List of variants in gene combination ANK2, LOC126807137 reported as likely benign for heart conduction disease

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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: 1

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HGVS	dbSNP	gnomAD frequency
NM_001148.6(ANK2):c.7132G>A (p.Glu2378Lys)	rs141191319	0.00222

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