ClinVar Miner

Submissions for variant NM_058172.6(ANTXR2):c.636+54T>A

gnomAD frequency: 0.61408  dbSNP: rs10745242
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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 RCV001554006 SCV001775146 benign Hyaline fibromatosis syndrome 2021-07-14 criteria provided, single submitter clinical testing
GeneDx RCV001647431 SCV001861050 benign not provided 2018-11-10 criteria provided, single submitter clinical testing

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