ClinVar Miner

Submissions for variant NM_031471.6(FERMT3):c.1914G>C (p.Ser638=)

dbSNP: rs192928228
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001515669 SCV001723798 benign Leukocyte adhesion deficiency 3 2023-12-07 criteria provided, single submitter clinical testing

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