ClinVar Miner

Submissions for variant NM_001130144.3(LTBP3):c.2033_2041delinsCTT (p.Asn678_Gly681delinsThrCys)

dbSNP: rs1856424871
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
University of Washington Center for Mendelian Genomics, University of Washington RCV001291429 SCV001479931 confers sensitivity Heritable Thoracic Aortic Disease no assertion criteria provided research

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