ClinVar Miner

Submissions for variant NM_000129.4(F13A1):c.1217-23C>T

gnomAD frequency: 0.26684  dbSNP: rs5978
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001611337 SCV001834942 benign not provided 2018-11-10 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001702933 SCV001933774 benign Factor XIII, A subunit, deficiency of 2021-08-10 criteria provided, single submitter clinical testing

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