ClinVar Miner

Submissions for variant NM_058172.6(ANTXR2):c.1042-114G>A

dbSNP: rs4444771
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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 RCV001554005 SCV001775145 benign Hyaline fibromatosis syndrome 2021-07-14 criteria provided, single submitter clinical testing
GeneDx RCV001709738 SCV001936914 benign not provided 2018-11-10 criteria provided, single submitter clinical testing

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