ClinVar Miner

Submissions for variant NM_016363.5(GP6):c.576A>G (p.Ser192=)

dbSNP: rs1654425
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000250060 SCV000306494 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001683006 SCV001900863 benign not provided 2018-11-12 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001701960 SCV001933899 benign Platelet-type bleeding disorder 11 2021-08-10 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001683006 SCV003340075 benign not provided 2024-01-31 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001683006 SCV005312869 benign not provided criteria provided, single submitter not provided

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