The broad classification of the phenotype (e.g., **Protein level**, **Metabolite level**).
Phenotype
The human-readable name of the trait or measurement studied.
#Samples
The total number of samples (individuals) included in the GWAS for this phenotype.
GCλ0.01
**Genomic Control (GC) λ at p-value 10-2**. This value indicates the degree of p-value inflation, where values near **1.0** suggest minimal population structure issues.
#Loci<5e-8
The number of **independent genomic regions (loci)** that contain variants reaching the standard genome-wide significance threshold (p < 5 × 10-8).
Top variant
The variant with the smallest (most significant) p-value across the entire genome for this phenotype.
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.
Nearest Gene(s)
The gene or genes closest to the position of the Top variant.