ClinVar Miner

Submissions for variant NM_001134831.2(AHI1):c.3110-22_3110-19del

dbSNP: rs71725890
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Preventiongenetics, part of Exact Sciences RCV000248025 SCV000312885 likely benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001711572 SCV000728911 benign not provided 2018-05-10 criteria provided, single submitter clinical testing
Invitae RCV001511771 SCV001719067 benign Familial aplasia of the vermis 2024-01-31 criteria provided, single submitter clinical testing

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