ClinVar Miner

Submissions for variant NM_020812.4(DOCK6):c.4350G>C (p.Leu1450=)

gnomAD frequency: 0.00002  dbSNP: rs763073235
Minimum review status: Collection method:
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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
CeGaT Center for Human Genetics Tuebingen RCV000996763 SCV001151676 uncertain significance not provided 2016-05-01 criteria provided, single submitter clinical testing
Invitae RCV000996763 SCV002459454 likely benign not provided 2022-01-06 criteria provided, single submitter clinical testing

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