ClinVar Miner

Submissions for variant NM_199242.3(UNC13D):c.1596+15C>G

dbSNP: rs574478720
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000292491 SCV000406667 uncertain significance Familial hemophagocytic lymphohistiocytosis 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002056630 SCV002473562 likely benign Familial hemophagocytic lymphohistiocytosis 3 2023-12-23 criteria provided, single submitter clinical testing

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