ClinVar Miner

Submissions for variant NM_001365999.1(SZT2):c.6508+16G>T

dbSNP: rs2782648
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000248361 SCV000312496 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001651208 SCV001864903 benign not provided 2018-07-15 criteria provided, single submitter clinical testing
Invitae RCV001651208 SCV002403690 benign not provided 2024-02-01 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003343734 SCV004049345 benign Developmental and epileptic encephalopathy, 18 2023-04-11 criteria provided, single submitter clinical testing

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