ClinVar Miner

Submissions for variant NM_000199.5(SGSH):c.88+23C>G

dbSNP: rs77032342
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 RCV000676158 SCV001841384 benign not provided 2018-07-06 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV000676158 SCV000801909 likely benign not provided 2018-02-08 no assertion criteria provided clinical testing

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