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

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_004820.5(CYP7B1):c.1456C>T (p.Arg486Cys)	rs116171274	0.00051
NM_004820.5(CYP7B1):c.1250G>A (p.Arg417His)	rs121908611	0.00006
NM_004820.5(CYP7B1):c.1150del (p.Asp384fs)	rs2129629942
NM_004820.5(CYP7B1):c.1249C>T (p.Arg417Cys)	rs367916692
NM_004820.5(CYP7B1):c.1354C>T (p.Arg452Ter)	rs769676029
NM_004820.5(CYP7B1):c.730A>T (p.Lys244Ter)

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