ClinVar Miner

Submissions for variant NM_005656.4(TMPRSS2):c.478G>A (p.Val160Met)

gnomAD frequency: 0.25326  dbSNP: rs12329760
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001668689 SCV001884839 benign not provided 2021-02-26 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 32867305)
Breakthrough Genomics, Breakthrough Genomics RCV001668689 SCV005310652 benign not provided criteria provided, single submitter not provided
HLA Laboratory, Instituto Nacional de Enfermedades Respiratorias Ismael Cosio Villegas RCV003401574 SCV004102841 uncertain significance Associated with severe COVID-19 disease 2023-07-01 no assertion criteria provided research

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