ClinVar Miner

Submissions for variant NM_001003787.4(STRADA):c.190C>T (p.Pro64Ser)

dbSNP: rs55695051
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Bioinformatics Core, Luxembourg Center for Systems Biomedicine RCV000656058 SCV000588334 pathogenic Childhood epilepsy with centrotemporal spikes 2017-01-01 no assertion criteria provided case-control CAADphred>15

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