ClinVar Miner

Submissions for variant NM_016363.5(GP6):c.*693A>G

gnomAD frequency: 0.74079  dbSNP: rs1654412
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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 RCV000254108 SCV000306486 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001683003 SCV001902118 benign not provided 2018-11-12 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001702383 SCV001933890 benign Platelet-type bleeding disorder 11 2021-08-10 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001683003 SCV003201502 benign not provided 2024-01-31 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001683003 SCV005312847 benign not provided criteria provided, single submitter not provided

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