ClinVar Miner

Submissions for variant NM_001692.4(ATP6V1B1):c.367+10A>T

dbSNP: rs1572919668
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000900923 SCV001045267 likely benign not provided 2023-09-21 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002502656 SCV002805432 likely benign Renal tubular acidosis with progressive nerve deafness 2021-07-27 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000900923 SCV005257015 likely benign not provided criteria provided, single submitter not provided

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