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GWAS ID | Year | Trait | Consortium | Sample size | Number of SNPs |
---|---|---|---|---|---|
finn-b-H7_KERATOCONUS | 2021 | Hereditary corneal dystrophies | NA | — | 16,380,407 |
finn-b-D3_HEREDOTHCLOFACTORS | 2021 | Hereditary deficiency of other clotting factors | NA | — | 16,380,461 |
finn-b-G6_HEREMOSEN | 2021 | Hereditary monor and sensory neuropathy | NA | — | 16,380,463 |
finn-b-H7_HEREDRETINADYST | 2021 | Hereditary retinal dystrophy | NA | — | 16,380,399 |
finn-b-K11_HERNIA | 2021 | Hernia | NA | — | 16,380,466 |
Data overview
The GWAS summary datasets are currently organised into the following 18 batches: