Variants in gene IVD with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_002225.5(IVD):c.*2285C>G	rs114657778	0.01453
NM_002225.5(IVD):c.-48G>A	rs114259808	0.01080
NM_002225.5(IVD):c.88C>T (p.His30Tyr)	rs73383128	0.00938
NM_002225.5(IVD):c.551-18C>T	rs142064071	0.00363
NM_002225.5(IVD):c.891G>A (p.Ala297=)	rs138427412	0.00069
NM_002225.5(IVD):c.234+16C>T	rs750473075	0.00025
NM_002225.5(IVD):c.1122C>T (p.Asp374=)	rs372504234	0.00005

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