Variants in gene BCS1L with conflicting interpretations "likely pathogenic" and "pathogenic"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (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: 16

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HGVS	dbSNP	gnomAD frequency
NM_001079866.2(BCS1L):c.205C>T (p.Arg69Cys)	rs377025174	0.00011
NM_001079866.2(BCS1L):c.550C>T (p.Arg184Cys)	rs121908578	0.00011
NM_001079866.2(BCS1L):c.325C>T (p.Arg109Trp)	rs141257714	0.00009
NM_001079866.2(BCS1L):c.547C>T (p.Arg183Cys)	rs144885874	0.00008
NM_001079866.2(BCS1L):c.871C>T (p.Arg291Ter)	rs201454788	0.00005
NM_001079866.2(BCS1L):c.355C>T (p.Arg119Ter)	rs770749420	0.00004
NM_001079866.2(BCS1L):c.598C>T (p.Arg200Ter)	rs776838028	0.00004
NM_001079866.2(BCS1L):c.134G>A (p.Arg45His)	rs754414354	0.00001
NM_001079866.2(BCS1L):c.349C>T (p.Arg117Ter)	rs777735526	0.00001
NM_001079866.2(BCS1L):c.889+1G>T	rs1057516346	0.00001
NM_001079866.2(BCS1L):c.917G>A (p.Arg306His)	rs1280810181	0.00001
NM_001079866.2(BCS1L):c.320+1G>T	rs386833856
NM_001079866.2(BCS1L):c.399del (p.Glu133fs)	rs751484879
NM_001079866.2(BCS1L):c.642G>A (p.Trp214Ter)	rs754414954
NM_001079866.2(BCS1L):c.703G>A (p.Gly235Arg)	rs368486097
NM_001079866.2(BCS1L):c.821del (p.Pro274fs)	rs760559534

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