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

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) 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.334C>T (p.Arg112Ter)	rs200737038	0.00007
NM_004820.5(CYP7B1):c.1061G>A (p.Ser354Asn)	rs753708048	0.00001
NM_004820.5(CYP7B1):c.1082G>A (p.Arg361Gln)	rs139816673
NM_004820.5(CYP7B1):c.1346G>A (p.Cys449Tyr)	rs761060634

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