ClinVar Miner

Submissions for variant NM_000039.3(APOA1):c.368C>T (p.Pro123Leu)

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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 RCV005044322 SCV005680696 uncertain significance Familial amyloid polyneuropathy, Iowa type; Hypoalphalipoproteinemia, primary, 2; Hypoalphalipoproteinemia, primary, 2, intermediate 2024-06-04 criteria provided, single submitter clinical testing

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