ClinVar Miner

Submissions for variant NM_014159.7(SETD2):c.71+10A>G

gnomAD frequency: 0.00003  dbSNP: rs776271538
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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 RCV003768740 SCV001021054 likely benign Luscan-Lumish syndrome 2023-03-13 criteria provided, single submitter clinical testing

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