ClinVar Miner

Submissions for variant NM_000129.4(F13A1):c.1217-24C>T

gnomAD frequency: 0.12083  dbSNP: rs5977
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001662972 SCV001872247 benign not provided 2021-06-19 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001702223 SCV001933785 benign Factor XIII, A subunit, deficiency of 2021-08-10 criteria provided, single submitter clinical testing

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