| Database: Data sets | Filters | Attributes |
|---|---|---|
| Ensembl Variation 61: Homo sapiens variation (dbSNP 132;ENSEMBL) | Limit to variants with these IDs dbSNP rs IDs: rs348, rs362, rs364, rs565, rs645 | Variation ID |
| Chromosome name | ||
| Position on chromosome (bp) | ||
| Ensembl Gene ID | ||
| Ensembl Genes 61: Homo sapiens genes (GRCh37.p2) | HGNC ID | |
| HGNC symbol |
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