Top Hits

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This page shows only the peaks with a p-value < 10-6. Variants are hidden if any variant within 500kb in the same phenotype has a smaller p-value. Only the top 2000 variants of each phenotype are considered. This table is limited to the top 1000 hits, but the download button includes all hits.


Category Phenotype Top variant in locus P-value (GC corrected) Raw P-value MAF Nearest Gene(s)

Column Descriptions

Category
The broad classification of the phenotype (e.g., **Protein level**, **Metabolite level**).
Phenotype
The human-readable name of the trait or measurement studied.
Top variant in locus
The variant with the smallest (most significant) p-value in the associated genomic region (locus).
P-value (GC corrected)
The genomic control–adjusted p-value of the Top variant, used for ranking and significance assessment.
Raw P-value
The original association p-value of the Top variant before genomic control correction.
MAF
**Minor Allele Frequency**. The frequency of the least common allele for this variant in the study population.
Nearest Gene(s)
The gene or genes closest to the position of the Top variant in the locus.