ClinVar Miner

Submissions for variant NM_005529.7(HSPG2):c.9329-8_9329-7delinsTT

dbSNP: rs386629395
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics Inc RCV000992151 SCV001144191 benign not provided 2019-03-27 criteria provided, single submitter clinical testing
Invitae RCV000992151 SCV001657615 likely benign not provided 2024-01-31 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000992151 SCV002058037 benign not provided 2023-11-29 criteria provided, single submitter clinical testing

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