Variants in gene BCS1L with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) 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_001079866.2(BCS1L):c.775T>A (p.Ser259Thr)	rs77729067	0.00132
NM_001079866.2(BCS1L):c.1000G>A (p.Val334Ile)	rs146731467	0.00086
NM_001079866.2(BCS1L):c.64C>T (p.Leu22=)	rs777854606	0.00027
NM_001079866.2(BCS1L):c.822G>A (p.Pro274=)	rs112329020	0.00014
NM_001079866.2(BCS1L):c.201C>T (p.Leu67=)	rs142540289	0.00007
NM_001079866.2(BCS1L):c.217C>T (p.Arg73Cys)	rs140812286	0.00006
NM_001079866.2(BCS1L):c.258T>C (p.His86=)	rs886055627	0.00001
NM_001079866.2(BCS1L):c.768C>G (p.Leu256=)	rs781666793	0.00001
NM_001079866.2(BCS1L):c.326G>A (p.Arg109Gln)
NM_001079866.2(BCS1L):c.349C>A (p.Arg117=)	rs777735526

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