ClinVar Miner

Submissions for variant NM_001077653.2(TBX20):c.995del (p.Pro332fs) (rs1554284604)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Centre for Genomic and Experimental Medicine,University of Edinburgh RCV000656080 SCV000598629 pathogenic Hypoplastic left heart syndrome 2015-12-01 no assertion criteria provided research
Centre for Genomic and Experimental Medicine,University of Edinburgh RCV000656081 SCV000598630 pathogenic Hypoplastic right heart syndrome 2015-12-01 no assertion criteria provided research
Centre for Genomic and Experimental Medicine,University of Edinburgh RCV000656082 SCV000598631 pathogenic Wolff-Parkinson-White pattern 2015-12-01 no assertion criteria provided research

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