ClinVar Miner

Submissions for variant NM_198569.3(ADGRG6):c.1955+4A>C

gnomAD frequency: 0.00056  dbSNP: rs372735218
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mayo Clinic Laboratories, Mayo Clinic RCV001508204 SCV001714193 uncertain significance not provided 2019-12-16 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV001508204 SCV004160392 likely benign not provided 2022-05-01 criteria provided, single submitter clinical testing ADGRG6: BP4

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