Variants in gene CYP7B1 with conflicting interpretations "uncertain significance" and "likely pathogenic"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) 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_004820.5(CYP7B1):c.440G>A (p.Gly147Asp)	rs754730601	0.00001
NM_004820.5(CYP7B1):c.1460dup (p.Leu487fs)	rs776075679
NM_004820.5(CYP7B1):c.788T>G (p.Val263Gly)

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