| Variant Name | Allele Count | Allele Frequency | Associated Disease | Associated Gene |
|---|---|---|---|---|
| NM_000595.4:c.179C>A | ||||
| NR_003529.3:n.2698+1211A>G | ||||
| NG_052669.1:g.31204C>T | ||||
| NC_000010.11:g.44280376C>T | ||||
| NM_001242767.1:c.1260-4955G>A | ||||
| NM_018256.3:c.1195-225A>G | ||||
| NC_000001.11:g.55030366T>A | ||||
| NM_005475.3:c.784T>A | ||||
| NM_002973.4:c.252-14033G>C | ||||
| NM_021977.3:c.1289-261T>C |