ClinVar Miner

Submissions for variant NM_022788.5(P2RY12):c.36T>G (p.Gly12=)

gnomAD frequency: 0.88072  dbSNP: rs6809699
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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 RCV000245981 SCV000314127 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001668582 SCV001887904 benign not provided 2021-06-09 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001788179 SCV002029366 benign Platelet-type bleeding disorder 8 2021-09-05 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001668582 SCV003334631 benign not provided 2024-01-31 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001668582 SCV005305150 benign not provided criteria provided, single submitter not provided

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