ClinVar Miner

Submissions for variant NM_020361.5(CPA6):c.1127-25_1127-24dup

dbSNP: rs60236534
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
Illumina Laboratory Services, Illumina RCV000296209 SCV000474739 uncertain significance Familial temporal lobe epilepsy 2 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004696087 SCV005195992 uncertain significance not provided criteria provided, single submitter not provided

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