ClinVar Miner

Submissions for variant NM_000552.5(VWF):c.2510C>A (p.Ala837Asp)

gnomAD frequency: 0.00739  dbSNP: rs75645183
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
Quest Diagnostics Nichols Institute San Juan Capistrano RCV003478761 SCV001469938 benign not provided 2023-09-09 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV003478761 SCV004226292 uncertain significance not provided 2022-11-30 criteria provided, single submitter clinical testing BP4
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV003478761 SCV004562374 benign not provided 2023-09-21 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV003478761 SCV005236795 benign not provided criteria provided, single submitter not provided

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