ClinVar Miner

Submissions for variant NM_001134831.2(AHI1):c.2037-77G>A

dbSNP: rs737561
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001548862 SCV001768851 benign Joubert syndrome 3 2021-07-14 criteria provided, single submitter clinical testing
GeneDx RCV001655871 SCV001869801 benign not provided 2018-06-26 criteria provided, single submitter clinical testing

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