ClinVar Miner

Submissions for variant NM_001029883.3(PCARE):c.2121A>T (p.Pro707=)

gnomAD frequency: 0.00049  dbSNP: rs199992183
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
Invitae RCV001394951 SCV001596649 likely benign not provided 2024-01-12 criteria provided, single submitter clinical testing

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