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: 2
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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)
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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