ClinVar Miner

Submissions for variant NM_015073.3(SIPA1L3):c.5203-29G>A

dbSNP: rs74573108
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001682183 SCV001902524 benign not provided 2018-06-29 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001807505 SCV002055253 benign Cataract 45 2021-07-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001682183 SCV005308539 benign not provided criteria provided, single submitter not provided

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