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De-identified GWAS summary statistics for a single genomic region. Sample names, variant positions, and identifiers have been randomized; they do not correspond to any real locus or study.

Format

A data frame with 2,828 rows and 8 columns:

variant_id

Character. Synthetic variant identifier (chrom:pos:A1:A2).

chrom

Character. Chromosome label.

pos

Integer. Genomic position (synthetic).

A1

Character. Effect allele.

A2

Character. Other allele.

beta

Numeric. GWAS effect size estimate.

se

Numeric. Standard error of the effect size.

z

Numeric. Z-score (beta / se).

Examples

data(gwas_sumstats_example)
head(gwas_sumstats_example)
#>           variant_id chrom      pos A1 A2    beta     se          z
#> 1 chr22:32119788:T:C chr22 32119788  T  C -0.0089 0.0111 -0.8018018
#> 2 chr22:32119867:T:G chr22 32119867  T  G -0.0089 0.0111 -0.8018018
#> 3 chr22:32119961:T:G chr22 32119961  T  G  0.0236 0.0083  2.8433735
#> 4 chr22:32120053:T:C chr22 32120053  T  C -0.0217 0.0246 -0.8821138
#> 5 chr22:32120593:A:G chr22 32120593  A  G -0.0232 0.0246 -0.9430894
#> 6 chr22:32120636:T:C chr22 32120636  T  C  0.0045 0.0141  0.3191489