Variants in gene CPT2 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000098.3(CPT2):c.1436A>T (p.Tyr479Phe)	rs749895856	0.00010
NM_000098.3(CPT2):c.691C>T (p.Arg231Trp)	rs373638740	0.00004
NM_000098.3(CPT2):c.1115A>G (p.His372Arg)	rs1212235186	0.00001
NM_000098.3(CPT2):c.461A>G (p.Asn154Ser)	rs772269793	0.00001
NM_000098.3(CPT2):c.481C>T (p.Arg161Trp)	rs756839691	0.00001
NM_000098.3(CPT2):c.674G>A (p.Arg225His)	rs794727616	0.00001
NM_000098.3(CPT2):c.1810C>T (p.Pro604Ser)	rs1645443275
NM_000098.3(CPT2):c.1822G>C (p.Asp608His)	rs780286639
NM_000098.3(CPT2):c.371G>C (p.Arg124Pro)	rs1131691925
NM_000098.3(CPT2):c.577C>T (p.Arg193Cys)	rs375968699

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