ClinVar Miner

Submissions for variant NM_000264.5(PTCH1):c.*1884CGTG[4]

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
CeGaT Center for Human Genetics Tuebingen RCV002512382 SCV002821950 benign not provided 2023-05-01 criteria provided, single submitter clinical testing PTCH1: BS1, BS2

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