ClinVar Miner

Submissions for variant NM_182961.4(SYNE1):c.23627+29G>A

gnomAD frequency: 0.04024  dbSNP: rs41292868
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 RCV000244494 SCV000315139 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001683129 SCV001902053 benign not provided 2018-06-28 criteria provided, single submitter clinical testing

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