ClinVar Miner

Submissions for variant NM_020812.4(DOCK6):c.3895-7C>T

gnomAD frequency: 0.00026  dbSNP: rs368322024
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
Labcorp Genetics (formerly Invitae), Labcorp RCV002111206 SCV002382121 likely benign not provided 2024-01-11 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002111206 SCV005041610 uncertain significance not provided 2024-04-01 criteria provided, single submitter clinical testing DOCK6: PM2, BP4

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