ClinVar Miner

Submissions for variant NM_001142800.2(EYS):c.3164+8T>C

gnomAD frequency: 0.00003  dbSNP: rs1385606496
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV000762419 SCV000892734 uncertain significance not provided 2018-06-01 criteria provided, single submitter clinical testing
Invitae RCV000762419 SCV001683148 likely benign not provided 2023-12-02 criteria provided, single submitter clinical testing

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