ClinVar Miner

Submissions for variant NM_001365536.1(SCN9A):c.2874+11_2874+13delinsTT

dbSNP: rs1553487749
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 RCV000244754 SCV000309309 likely benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001640527 SCV001855345 benign not provided 2015-03-03 criteria provided, single submitter clinical testing

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