Variants in gene CPT1A with conflicting interpretations "likely pathogenic" and "pathogenic"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (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: 16

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HGVS	dbSNP	gnomAD frequency
NM_001876.4(CPT1A):c.1364A>C (p.Lys455Thr)	rs189174414	0.00020
NM_001876.4(CPT1A):c.1163+1G>A	rs148059333	0.00005
NM_001876.4(CPT1A):c.1386del (p.Phe462fs)	rs753776604	0.00002
NM_001876.4(CPT1A):c.1792C>T (p.Arg598Ter)	rs773153659	0.00001
NM_001876.4(CPT1A):c.2129G>A (p.Gly710Glu)	rs80356780	0.00001
NM_001876.4(CPT1A):c.589G>T (p.Glu197Ter)	rs1211665230	0.00001
NM_001876.4(CPT1A):c.727C>T (p.Arg243Ter)	rs779893091	0.00001
NM_001876.4(CPT1A):c.1163+2T>C	rs1555229059
NM_001876.4(CPT1A):c.1493A>G (p.Tyr498Cys)	rs80356791
NM_001876.4(CPT1A):c.1876-1G>A	rs80356798
NM_001876.4(CPT1A):c.1879G>T (p.Glu627Ter)
NM_001876.4(CPT1A):c.1997_1998insAAAA (p.Tyr666Ter)	rs1057516800
NM_001876.4(CPT1A):c.2018_2022del (p.Pro672_Phe673insTer)	rs1163935346
NM_001876.4(CPT1A):c.2071C>T (p.Gln691Ter)	rs765161206
NM_001876.4(CPT1A):c.222C>A (p.Tyr74Ter)	rs398123654
NM_001876.4(CPT1A):c.298C>T (p.Gln100Ter)	rs80356774

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