ClinVar Miner

Submissions for variant NM_020632.3(ATP6V0A4):c.816+19C>T

gnomAD frequency: 0.00643  dbSNP: rs80076422
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
Labcorp Genetics (formerly Invitae), Labcorp RCV002084246 SCV002430118 benign not provided 2024-01-25 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002494338 SCV002803703 benign Renal tubular acidosis, distal, 3, with or without sensorineural hearing loss 2021-08-09 criteria provided, single submitter clinical testing

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