ClinVar Miner

Submissions for variant NM_007363.5(NONO):c.154+11G>C

gnomAD frequency: 0.01069  dbSNP: rs142366840
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002126922 SCV002409670 benign not provided 2024-01-25 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002507997 SCV002796685 likely benign Syndromic X-linked intellectual disability 34 2021-09-13 criteria provided, single submitter clinical testing

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