ClinVar Miner

Submissions for variant NM_182914.3(SYNE2):c.18201+90C>T

gnomAD frequency: 0.44936  dbSNP: rs6573548
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 RCV001694515 SCV001908077 benign not provided 2018-07-09 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001694515 SCV005292643 benign not provided criteria provided, single submitter not provided

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