ClinVar Miner

Submissions for variant NM_001044385.3(TMEM237):c.80-18dup

dbSNP: rs747217784
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001517384 SCV001725868 benign Joubert syndrome 14 2023-11-27 criteria provided, single submitter clinical testing
GeneDx RCV001562967 SCV001785823 likely benign not provided 2020-09-30 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV001517384 SCV002795602 likely benign Joubert syndrome 14 2022-01-03 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV001562967 SCV004148415 likely benign not provided 2023-11-01 criteria provided, single submitter clinical testing TMEM237: BP4

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