ClinVar Miner

Submissions for variant NM_001244710.2(GFPT1):c.7+20G>T

gnomAD frequency: 0.00088  dbSNP: rs373299682
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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 RCV002108473 SCV002439776 likely benign Congenital myasthenic syndrome 12 2025-01-29 criteria provided, single submitter clinical testing

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