ClinVar Miner

List of variants in gene combination ACAD9, CFAP92 reported as likely pathogenic by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_014049.5(ACAD9):c.1674_1692+34del	rs2107664575
NM_014049.5(ACAD9):c.1805C>T (p.Ser602Phe)	rs2529107329

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