ClinVar Miner

Submissions for variant NM_013386.5(SLC25A24):c.398+45T>C

gnomAD frequency: 0.72989  dbSNP: rs490680
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001654172 SCV001863879 benign not provided 2021-05-14 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001807472 SCV002055904 benign Fontaine progeroid syndrome 2021-07-15 criteria provided, single submitter clinical testing

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