ClinVar Miner

Submissions for variant NM_000173.7(GP1BA):c.1321_1359del (p.415_427SEPAPSPTTPEPT[2])

dbSNP: rs1259394995
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000251606 SCV000302856 likely benign not specified criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV000251606 SCV000595025 benign not specified 2016-10-25 criteria provided, single submitter clinical testing

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