ClinVar Miner

Submissions for variant NM_001029883.3(PCARE):c.2191G>A (p.Val731Ile)

gnomAD frequency: 0.00010  dbSNP: rs201790782
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000592452 SCV000703482 uncertain significance not provided 2016-12-02 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000592452 SCV001034087 likely benign not provided 2024-10-28 criteria provided, single submitter clinical testing

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