ClinVar Miner

Submissions for variant NM_031471.6(FERMT3):c.1671-14T>C

gnomAD frequency: 0.00004  dbSNP: rs201170855
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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 RCV002188138 SCV002355361 benign Leukocyte adhesion deficiency 3 2024-01-16 criteria provided, single submitter clinical testing

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