Variants in gene CYP27A1 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000784.4(CYP27A1):c.1151C>T (p.Pro384Leu)	rs41272687	0.01478
NM_000784.4(CYP27A1):c.-6C>T	rs199891090	0.00673
NM_000784.4(CYP27A1):c.276C>T (p.Tyr92=)	rs141519183	0.00053
NM_000784.4(CYP27A1):c.1419C>T (p.Val473=)	rs138596741	0.00037
NM_000784.4(CYP27A1):c.789C>T (p.Pro263=)	rs143600636	0.00019
NM_000784.4(CYP27A1):c.1184+9G>T	rs200457116	0.00016
NM_000784.4(CYP27A1):c.504A>T (p.Pro168=)	rs142623022	0.00016
NM_000784.4(CYP27A1):c.578G>A (p.Arg193Gln)	rs181649030	0.00012
NM_000784.4(CYP27A1):c.792G>A (p.Val264=)	rs144018609	0.00010
NM_000784.4(CYP27A1):c.1263+10del	rs765426068

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