ClinVar Miner

Submissions for variant NM_000039.3(APOA1):c.-21+5G>A

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005049993 SCV005680715 likely benign Familial amyloid polyneuropathy, Iowa type; Hypoalphalipoproteinemia, primary, 2; Hypoalphalipoproteinemia, primary, 2, intermediate 2024-01-23 criteria provided, single submitter clinical testing

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