Variant Annotation
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This module allows you to get detailed annotations for one or more variants. If the results are not what you have expected, please check the "Report" tab for details.
| Genome Assembly, Variant Set, Population, and Genome Annotation | ||
|---|---|---|
| Genome assembly: | Chromosome coordinates (and thus all genetic elements) are mapped to the selected human reference assembly. | |
| Variant set: | Linkage disequilibrium data and allele frequencies are computed for the selected variant set (and population where applicable). | |
| Population: | If a variant set contains more than one population, select the one that fits your study population best. | |
| Genome annotation: | Genetic elements are annotated based on data of the selected annotation dataset. | |
| Variants | ||
|---|---|---|
| Variants: |
For variants entered here, SNiPA provides functional annotations if available. In case you have already added variants to SNiPA's clipboard, these are available as a preselection. Please input one rs-identifier per line. |
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