ClinVar Miner

Submissions for variant NM_014272.5(ADAMTS7):c.640T>C (p.Ser214Pro)

gnomAD frequency: 0.32795  dbSNP: rs3825807
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
Breakthrough Genomics, Breakthrough Genomics RCV004715374 SCV005291301 benign not provided criteria provided, single submitter not provided
Department of Cardiology, Chinese Academy of Medical Sciences, Fuwai Hospital RCV001003456 SCV001161751 benign Three Vessel Coronary Disease no assertion criteria provided clinical testing

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