ClinVar Miner

Submissions for variant NM_020987.5(ANK3):c.6621C>T (p.Pro2207=)

gnomAD frequency: 0.00473  dbSNP: rs61732396
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
Labcorp Genetics (formerly Invitae), Labcorp RCV000965138 SCV001112398 benign not provided 2025-01-06 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000965138 SCV004125432 benign not provided 2022-12-01 criteria provided, single submitter clinical testing ANK3: BP4, BP7, BS1, BS2
Breakthrough Genomics, Breakthrough Genomics RCV000965138 SCV005322801 benign not provided criteria provided, single submitter not provided

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