ClinVar Miner

Submissions for variant NM_031471.6(FERMT3):c.161-11G>A

gnomAD frequency: 0.00143  dbSNP: rs188768294
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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 RCV001519095 SCV001727901 benign Leukocyte adhesion deficiency 3 2024-01-31 criteria provided, single submitter clinical testing

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