Human (GRCh37.p13)
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  • Global MAFAll
    Global MAF
  • ClassAll
    Class
  • Clinical SignificanceAll
    Clinical Significance
  • ConsequencesAll
    Consequences
  • LocationAll
    Location
  • Sour­ceAll
    Sour­ce
  • Evid­enceAll
    Evid­ence
  • ClinVar IDAll
    ClinVar ID
  • PhenotypesAll
    Phenotypes
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  • Variant ID
  • Chr: bp
  • Alle­les
  • Glo­bal MAF
  • Class
  • Sour­ce
  • Evid­ence
  • Clin. Sig.
  • ClinVar ID
  • Consequence
  • Phenotype
Variant ID
Chr: bp
Alle­les
Glo­bal MAF
Class
Sour­ce
Evid­ence
Clin. Sig.
ClinVar ID
Consequence
Phenotype
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