Variant Name | Allele Count | Allele Frequency | Associated Disease | Associated Gene |
---|---|---|---|---|
NM_024006.6:c.106G>T | 0.005 | |||
NM_001348945.1:c.3645T>C | 0.597 | |||
NM_000769.4:c.681G>A | 0.151 | |||
NM_000767.5:c.516G>T | 0.31 | |||
NM_000771.4:c.1075A>C | 0.07071 | |||
NM_000852.4:c.313A>G | 0.3163 | |||
NM_018283.4:c.415C>T | 0.005 | |||
NM_000771.3:c.430C>T | 0.11 | |||
NM_000015.3:c.590G>A | 0.315 | |||
NM_004827.3:c.421C>A | 0.061 | |||
NM_006446.5:c.521T>C | 0.187 | |||
NM_000110.3:c.557A>G | 0.005 | |||
NM_001082.5:c.1297G>A | 0.4592 | |||
NM_000767.5:c.983T>C | 0.0101 | |||
NM_001348944.2:c.2677T>G | 0.611 | |||
NM_005845.5:c.3348G>C | 0.826 | |||
NM_001025195.2:c.431G>A | 0.02 | |||
NM_000770.3:c.1196A>G | 0.1364 | |||
NM_000771.3:c.449G>C | 0.02 | |||
NM_000463.2:c.211G>A | 0.005 | |||
NM_000015.3:c.282C>T | 0.3333 | |||
NM_001199633.1:c.1381C>T | 0.1111 | |||
NM_007120.3:c.142T>G | 0.1173 |