Variants in gene BCS1L 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: 8

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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.269G>A (p.Arg90His)	rs747956412	0.00004
NM_001079866.2(BCS1L):c.551G>A (p.Arg184His)	rs779504946	0.00003
NM_001079866.2(BCS1L):c.-50+405A>G	rs898301590	0.00002
NM_001079866.2(BCS1L):c.-49-539T>A	rs386833855
NM_001079866.2(BCS1L):c.295C>T (p.Pro99Ser)
NM_001079866.2(BCS1L):c.399del (p.Glu133fs)	rs751484879
NM_001079866.2(BCS1L):c.703G>A (p.Gly235Arg)	rs368486097

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