ClinVar Miner

Submissions for variant NM_000264.5(PTCH1):c.201+272T>C

dbSNP: rs1355619
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
GeneDx RCV001722700 SCV001949395 benign not provided 2018-06-26 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001722700 SCV005265055 benign not provided criteria provided, single submitter not provided

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