Variants in gene CPT2 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (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_000098.3(CPT2):c.1055T>G (p.Phe352Cys)	rs2229291	0.01469
NM_000098.3(CPT2):c.1767G>A (p.Thr589=)	rs77565483	0.01032
NM_000098.3(CPT2):c.302C>T (p.Ala101Val)	rs75939866	0.00675
NM_000098.3(CPT2):c.1578T>C (p.Gly526=)	rs113493395	0.00455
NM_000098.3(CPT2):c.1763C>G (p.Ser588Cys)	rs1871748	0.00353
NM_000098.3(CPT2):c.1806T>C (p.Phe602=)	rs147953465	0.00218
NM_000098.3(CPT2):c.353A>G (p.Asp118Gly)	rs148035648	0.00084
NM_000098.3(CPT2):c.588T>C (p.Pro196=)	rs140853350	0.00035
NM_000098.3(CPT2):c.1598T>C (p.Val533Ala)	rs144703247	0.00022
NM_000098.3(CPT2):c.1851T>C (p.His617=)	rs540322467	0.00011

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