| is a | gene |
| is | mentioned by |
| Full name | sodium channel, voltage-gated, type I, alpha subunit |
| Related | SCN2A, SCN3A, SCN4A, SCN5A, SCN7A, SCN8A, SCN9A, SCN10A, SCN11A |
| EntrezGene | 6323 |
| PheGenI | 6323 |
| VariationViewer | 6323 |
| ClinVar | SCN1A |
| GeneCards | SCN1A |
| dbSNP | 6323 |
| Diseases | SCN1A |
| SADR | 6323 |
| HugeNav | 6323 |
| wikipedia | SCN1A |
| google | SCN1A |
| gopubmed | SCN1A |
| EVS | SCN1A |
| HEFalMp | SCN1A |
| MyGene2 | SCN1A |
| 23andMe | SCN1A |
| UniProt | P35498 |
| Ensembl | ENSG00000144285 |
| OMIM | 182389 |
| # SNPs | 552 |
| | Max Magnitude | Chromosome position | Summary |
|---|
| rs10188577 | 0 | 166,059,387 | |
| rs1057517849 | 0 | 166,039,422 | |
| rs1057517862 | 0 | 166,038,128 | |
| rs1057517958 | 0 | 165,991,711 | |
| rs1057517959 | 0 | 166,041,284 | |
| rs1057518062 | 0 | 166,002,476 | |
| rs1057518094 | 0 | 166,047,707 | |
| rs1057518110 | 0 | 166,038,116 | |
| rs1057518112 | 0 | 166,037,781 | |
| rs1057518129 | 0 | 166,046,769 | |
| rs1057518229 | 0 | 166,009,823 | |
| rs1057518243 | 0 | 166,047,763 | |
| rs1057518252 | 0 | 165,991,993 | |
| rs1057518258 | 0 | 165,992,030 | |
| rs1057518325 | 0 | 166,037,795 | |
| rs1057518671 | 0 | 165,991,924 | |
| rs1057519529 | 0 | 166,043,864 | |
| rs1057519530 | 0 | 166,052,864 | |
| rs1057519531 | 0 | 166,052,945 | |
| rs1057519532 | 0 | 165,994,177 | |
| rs1057519533 | 0 | 165,994,184 | |
| rs1057519534 | 0 | 166,013,758 | |
| rs1057520486 | 0 | 166,037,771 | |
| rs1057521079 | 0 | 165,992,362 | |
| rs1057521080 | 0 | 166,037,903 | |
| rs1057521537 | 0 | 166,002,695 | |
| rs1057521746 | 0 | 166,009,753 | |
| rs1057523858 | 0 | 166,047,647 | |
| rs1057524737 | 0 | 166,047,622 | |
| rs1057524752 | 0 | 166,047,728 | |
| rs1060502183 | 0 | 166,002,520 | |
| rs1060502185 | 0 | 166,058,565 | |
| rs1060502187 | 0 | 166,058,641 | |
| rs1060502188 | 0 | 166,012,166 | |
| rs1060502190 | 0 | 166,002,489 | |
| rs1064793315 | 0 | 166,054,731 | |
| rs1064793678 | 0 | 166,052,896 | |
| rs1064794147 | 0 | 166,046,800 | |
| rs1064794251 | 0 | 165,991,497 | |
| rs1064794252 | 0 | 166,051,789 | |
| rs1064794495 | 0 | 166,015,706 | |
| rs1064794503 | 0 | 166,041,311 | |
| rs1064794508 | 0 | 166,041,332 | |
| rs1064794630 | 0 | 165,992,000 | |
| rs1064794634 | 0 | 166,056,406 | |
| rs1064794766 | 0 | 165,992,303 | |
| rs1064794913 | 0 | 166,045,072 | |
| rs1064795239 | 0 | 166,009,783 | |
| rs1064795303 | 0 | 166,002,645 | |
| rs1064795355 | 0 | 166,012,188 | |
Mutations in the SCN1A gene have been associated with Severe myoclonic epilepsy in infancy (SMEI) and Dravet syndrome, forms of epilepsy. Washington Post article [1] NCBI Bookshelf
