Variants in gene CYP7B1 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_004820.5(CYP7B1):c.122+19A>T	rs7842714	0.39118
NC_000008.11:g.64798895G>C	rs117576566	0.02967
NM_004820.5(CYP7B1):c.971G>A (p.Arg324His)	rs59035258	0.02701
NM_004820.5(CYP7B1):c.1464G>A (p.Leu488=)	rs114797034	0.00140

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