ClinVar Miner

Submissions for variant NM_006922.4(SCN3A):c.642G>A (p.Ala214=)

gnomAD frequency: 0.00048  dbSNP: rs575814709
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) RCV000153906 SCV000203519 uncertain significance not provided 2014-02-17 criteria provided, single submitter clinical testing
Invitae RCV000153906 SCV001717881 benign not provided 2023-12-11 criteria provided, single submitter clinical testing

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