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

Submission 1 (benign) minimum review status:		Submission 1 (benign) 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001079866.2(BCS1L):c.613G>A (p.Val205Ile)	rs148278887	0.00295
NM_001079866.2(BCS1L):c.775T>A (p.Ser259Thr)	rs77729067	0.00132
NM_001079866.2(BCS1L):c.126A>G (p.Ala42=)	rs144200704	0.00039
NM_001079866.2(BCS1L):c.461-9C>T	rs780651750	0.00021
NM_001079866.2(BCS1L):c.628G>A (p.Asp210Asn)	rs58447305

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