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Variants are colored by the putative impact of their most deleterious effect.
Effect impacts are colored as follows:
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:
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.
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