ClinVar Miner

Submissions for variant NM_020987.5(ANK3):c.2889C>T (p.Tyr963=)

gnomAD frequency: 0.00309  dbSNP: rs149682716
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000194063 SCV000246383 benign not specified 2017-04-24 criteria provided, single submitter clinical testing
Invitae RCV000888826 SCV001032479 benign not provided 2023-12-12 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000888826 SCV004125445 likely benign not provided 2023-09-01 criteria provided, single submitter clinical testing ANK3: BP4, BP7

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