ClinVar Miner

Submissions for variant NM_001289104.2(PRKCSH):c.1196+52A>G

gnomAD frequency: 0.16150  dbSNP: rs160841
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 RCV001538447 SCV001756098 benign not provided 2018-07-09 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001538447 SCV005312723 benign not provided criteria provided, single submitter not provided

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