ClinVar Miner

Submissions for variant NM_016363.5(GP6):c.709G>A (p.Glu237Lys)

dbSNP: rs1654416
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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 RCV000246602 SCV000306496 benign not specified criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001701893 SCV001933897 benign Platelet-type bleeding disorder 11 2021-08-10 criteria provided, single submitter clinical testing
GeneDx RCV001707583 SCV001936040 benign not provided 2018-11-12 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001707583 SCV003201509 benign not provided 2024-01-31 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001707583 SCV005312866 benign not provided criteria provided, single submitter not provided

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