ClinVar Miner

Variants with conflicting interpretations "pathogenic" from Center for Advanced Laboratory Medicine, UC San Diego Health, University of California San Diego and "likely pathogenic" from any submitter

Minimum review status of the submission from Center for Advanced Laboratory Medicine, UC San Diego Health, University of California San Diego: Collection method of the submission from Center for Advanced Laboratory Medicine, UC San Diego Health, University of California San Diego:
Minimum review status of the other submission: Collection method of the other submission:
ClinVar version:
Total variants with conflicting interpretations: 3
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HGVS dbSNP gnomAD frequency
NM_001267550.2(TTN):c.86821+2T>A rs397517735 0.00005
NM_000257.4(MYH7):c.709C>T (p.Arg237Trp) rs45516091 0.00001
NM_000256.3(MYBPC3):c.833del (p.Gly278fs) rs727503212

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