Table 1.
Variant ID | TraP | Gene ID | Phenotype associated with Gene | Ref |
---|---|---|---|---|
15-23062273-T-G | 0.949 | NIPA1 | Hereditary spastic paraplegia and association to Epilepsy | 29 |
18-40695437-G-A | 0.812 | RIT2 | Schizophrenia, synaptic signaling; weak PD | 31, 32 |
2-222428815-G-A | 0.438 | EPHA4 | ALS, neurogenesis; strong interaction with ARHGEF15 (a known epilepsy gene) | 33 |
14-23858626-T-C | 0.430 | MYH6 | Cardiomyopathy | |
3-42700087-G-A | 0.383 | ZBTB47 | Unknown | |
15-93472268-C-T | 0.358 | CHD2 | Epileptic encephalopathy | 27 |
13-52249316-A-G | 0.352 | WDFY2 | Unknown |
Genes associated with epilepsy are in bold and genes associated with other neurological disorders are underlined.