ClinVar Miner

Submissions for variant NM_000393.5(COL5A2):c.-16_-15insCTAACCCACATCAT

dbSNP: rs765138557
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000199452 SCV000249949 likely benign not specified 2015-03-03 criteria provided, single submitter clinical testing This variant was found in TAADV2-1

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