ClinVar Miner

Submissions for variant NM_005263.5(GFI1):c.115+10_115+29del

dbSNP: rs150506480
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000249753 SCV000310945 benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001522018 SCV001731479 benign Neutropenia, severe congenital, 2, autosomal dominant 2025-02-03 criteria provided, single submitter clinical testing
GeneDx RCV001610660 SCV001835264 benign not provided 2021-05-12 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001610660 SCV005878531 benign not provided 2024-10-17 criteria provided, single submitter clinical testing

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