ClinVar Miner

Submissions for variant NM_170665.4(ATP2A2):c.545-7C>T

gnomAD frequency: 0.00038  dbSNP: rs369585470
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics RCV004997225 SCV000840982 benign not specified 2024-07-02 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000710697 SCV001034975 benign not provided 2023-06-16 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002260041 SCV002539120 benign Acrokeratosis verruciformis of Hopf 2021-12-05 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002260040 SCV002539122 benign Keratosis follicularis 2021-12-05 criteria provided, single submitter clinical testing

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