Variants in gene ANK2 with conflicting interpretations "pathogenic" and "likely benign"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 3

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HGVS	dbSNP	gnomAD frequency
NM_001148.6(ANK2):c.11218C>A (p.Leu3740Ile)	rs35530544	0.00961
NM_001148.6(ANK2):c.11716C>T (p.Arg3906Trp)	rs121912706	0.00094
NM_001148.6(ANK2):c.4373A>G (p.Glu1458Gly)	rs72544141	0.00085

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