ClinVar Miner

Submissions for variant NM_001365276.2(TNXB):c.6842-24C>T

gnomAD frequency: 0.25409  dbSNP: rs2239689
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000241975 SCV000313382 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001668564 SCV001889100 benign not provided 2018-07-09 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001838597 SCV002098637 benign Ehlers-Danlos syndrome due to tenascin-X deficiency 2021-09-10 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001838598 SCV002098638 benign Vesicoureteral reflux 8 2021-09-10 criteria provided, single submitter clinical testing

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