Variable breakdown
panel_rs661348_t
Section and category
SNP Data.rs661348
Description
“Chromosome: 11, Base position: 1905292, Allele 1: T, Allele 2: C”
Additional information
| Metadata | |
|---|---|
| contents | Categorised |
| is_mandatory | No |
Data summary
Panel
| value | freq | pct_valid | pct_tot |
|---|---|---|---|
| Allele 2 homozygote | 19415 | 34.89 | 3.77 |
| Heterozygote | 26921 | 48.38 | 5.22 |
| Allele 1 homozygote | 9312 | 16.73 | 1.81 |
| <NA> | 459765 | NA | 89.20 |
Between-survey agreement
No agreement analysis available
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Page generated: 27-02-2024