Variants in gene combination ANK1, LOC124153154 with conflicting interpretations reported as "uncertain significance and "likely benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000037.4(ANK1):c.447G>T (p.Ala149=)	rs140550365	0.00025
NM_000037.4(ANK1):c.483G>A (p.Ala161=)	rs200639644	0.00009

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