ClinVar Miner

Submissions for variant NM_000297.4(PKD2):c.2568dup (p.Val857fs)

dbSNP: rs1578153553
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Blueprint Genetics RCV000788397 SCV000927488 likely pathogenic not provided 2017-12-04 criteria provided, single submitter clinical testing

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