ClinVar Miner

Submissions for variant NM_022081.6(HPS4):c.1956-32T>C

gnomAD frequency: 0.00756  dbSNP: rs189953957
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
PreventionGenetics, part of Exact Sciences RCV000253070 SCV000313937 likely benign not specified criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004703554 SCV005210232 likely benign not provided criteria provided, single submitter not provided

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