ClinVar Miner

Submissions for variant NM_001029883.3(PCARE):c.3783C>T (p.His1261=)

gnomAD frequency: 0.00014  dbSNP: rs201566996
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 RCV001435701 SCV001638527 likely benign not provided 2023-12-10 criteria provided, single submitter clinical testing

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