rs4363087
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4363087(C;C) |
| Make rs4363087(C;T) |
| Make rs4363087(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 73703866 |
| Gene | LOC105375350, STX1A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4363087 |
| dbSNP (classic) | rs4363087 |
| ClinGen | rs4363087 |
| ebi | rs4363087 |
| HLI | rs4363087 |
| Exac | rs4363087 |
| Gnomad | rs4363087 |
| Varsome | rs4363087 |
| LitVar | rs4363087 |
| Map | rs4363087 |
| PheGenI | rs4363087 |
| Biobank | rs4363087 |
| 1000 genomes | rs4363087 |
| hgdp | rs4363087 |
| ensembl | rs4363087 |
| geneview | rs4363087 |
| scholar | rs4363087 |
| rs4363087 | |
| pharmgkb | rs4363087 |
| gwascentral | rs4363087 |
| openSNP | rs4363087 |
| 23andMe | rs4363087 |
| SNPshot | rs4363087 |
| SNPdbe | rs4363087 |
| MSV3d | rs4363087 |
| GWAS Ctlg | rs4363087 |
| GMAF | 0.3884 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19368856] Contribution of syntaxin 1A to the genetic susceptibility to migraine: A case -- control association study in the Spanish population
[PMID 22250207] Association analysis of STX1A gene variants in common forms of migraine.
[PMID 23572023
] Clinical and molecular characterization of the potential CF disease modifier syntaxin 1A
