ClinVar Miner

Submissions for variant NM_020812.4(DOCK6):c.1761+6T>C

gnomAD frequency: 0.00016  dbSNP: rs200659753
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
Invitae RCV000963381 SCV001110532 benign not provided 2024-01-14 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000963381 SCV004137847 likely benign not provided 2023-10-01 criteria provided, single submitter clinical testing DOCK6: BP4, BS1

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