Unknown
| Variant Name | Allele Count | Allele Frequency | Associated Disease | Associated Gene |
|---|---|---|---|---|
| NM_001171.5:c.3803G>A | ||||
| NM_004827.3:c.421C>A | ||||
| NM_000761.5:c.1548T>C | ||||
| NM_000106.6:c.100C>T | ||||
| NC_000022.11:g.42132969C>T | ||||
| NM_001460.5:c.337del | ||||
| NM_001460.5:c.1239T>G | ||||
| NM_001460.3:c.211_213dup | ||||
| NM_001460.5:c.242T>C | ||||
| NM_001460.5:c.941A>G | ||||
| NM_016818.3:c.973+672G>A | ||||
| NM_006894.6:c.855C>T |