ClinVar Miner

Submissions for variant NM_001044385.3(TMEM237):c.75-8C>T

gnomAD frequency: 0.00003  dbSNP: rs1274569461
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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 RCV000931420 SCV001077086 likely benign Joubert syndrome 14 2022-01-07 criteria provided, single submitter clinical testing

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