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Variants are colored by the putative impact of their most deleterious effect.

Effect impacts are colored as follows:

  • High
  • Moderate
  • Low
  • Modifier
  • Not Reported

dbSNP tracks were annotated using the snpEff genetic variant annotation and effect prediction toolbox; ADSP tracks were annotated by the ADSP Annotation Working Group, using Ensembl's VEP v80 variant effect prediction tool.

Click on a variant for full details.

The y-axis represents the transformed -log10 p-value. Variants are colored by the relative significance of the trait association as follows:

  • -log10p
  • 3
  • 6
  • 9
  • 12

The y-axis is capped at a minimum p-value of 1 x 10-15 (max -log10 p = 15). Scores exceeding that value are drawn in blue ; non-significant variants (p-value > 0.05) are drawn in grey .

Mouse-over dots to view the p-value support for the variant-trait association.

Click on a variant to view its record page.

To enhance readability, functional genomics tracks are colored by type.

  • Histone Modification Site
  • Transcription Factor Binding Site
  • DNase Hypersensitivity Site
  • Expressed Enhancer Region