ClinVar Miner

Submissions for variant NM_007118.4(TRIO):c.6611A>G (p.Lys2204Arg)

dbSNP: rs141648983
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000899520 SCV001043795 likely benign not provided 2019-12-31 criteria provided, single submitter clinical testing
GeneDx RCV000899520 SCV001911869 benign not provided 2019-06-07 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV001818740 SCV002067671 likely benign not specified 2019-09-24 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000899520 SCV004154019 likely benign not provided 2024-06-01 criteria provided, single submitter clinical testing TRIO: BS1

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