ClinVar Miner

Submissions for variant NM_031471.6(FERMT3):c.1079+8G>T

gnomAD frequency: 0.00001  dbSNP: rs568273430
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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 RCV001419316 SCV001621565 likely benign Leukocyte adhesion deficiency 3 2023-09-11 criteria provided, single submitter clinical testing

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