ClinVar Miner

Submissions for variant NM_005529.7(HSPG2):c.8910+77T>C

gnomAD frequency: 0.03847  dbSNP: rs75779078
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 RCV001616410 SCV001840120 benign not provided 2018-08-25 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001616410 SCV005286252 benign not provided criteria provided, single submitter not provided

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