ClinVar Miner

Submissions for variant NM_182961.4(SYNE1):c.10650C>T (p.Asn3550=)

gnomAD frequency: 0.00001  dbSNP: rs772377391
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
Eurofins Ntd Llc (ga) RCV000593486 SCV000704198 uncertain significance not provided 2016-12-06 criteria provided, single submitter clinical testing
Athena Diagnostics RCV000593486 SCV001475585 likely benign not provided 2019-10-23 criteria provided, single submitter clinical testing

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