ClinVar Miner

Submissions for variant NM_001365276.2(TNXB):c.2516-17_2516-15del

dbSNP: rs199775035
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001657634 SCV001866240 benign not provided 2018-10-01 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002495980 SCV002805808 benign Ehlers-Danlos syndrome due to tenascin-X deficiency; Vesicoureteral reflux 8 2021-11-29 criteria provided, single submitter clinical testing

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