Variants in gene CYP7B1 with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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.1464G>A (p.Leu488=)	rs114797034	0.00140
NM_004820.5(CYP7B1):c.94G>T (p.Ala32Ser)	rs181854355	0.00056
NM_004820.5(CYP7B1):c.123-19dup	rs8192895
NM_004820.5(CYP7B1):c.260-15dup	rs8192896

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