ClinVar Miner

Submissions for variant NM_020987.5(ANK3):c.1690-15dup

dbSNP: rs34796699
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
Mendelics RCV000988367 SCV001138055 benign Intellectual disability-hypotonia-spasticity-sleep disorder syndrome 2019-05-28 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002067580 SCV002423976 benign not provided 2024-11-05 criteria provided, single submitter clinical testing

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