ClinVar Miner

Submissions for variant NM_000129.4(F13A1):c.521G>T (p.Ser174Ile)

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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 RCV005033451 SCV005673221 uncertain significance Factor XIII, A subunit, deficiency of; Thrombophilia due to thrombin defect; Myocardial infarction, susceptibility to 2024-03-05 criteria provided, single submitter clinical testing

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