rs2228607
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2228607(C;C) |
| Make rs2228607(C;T) |
| Make rs2228607(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 73708593 |
| Gene | STX1A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2228607 |
| dbSNP (classic) | rs2228607 |
| ClinGen | rs2228607 |
| ebi | rs2228607 |
| HLI | rs2228607 |
| Exac | rs2228607 |
| Gnomad | rs2228607 |
| Varsome | rs2228607 |
| LitVar | rs2228607 |
| Map | rs2228607 |
| PheGenI | rs2228607 |
| Biobank | rs2228607 |
| 1000 genomes | rs2228607 |
| hgdp | rs2228607 |
| ensembl | rs2228607 |
| geneview | rs2228607 |
| scholar | rs2228607 |
| rs2228607 | |
| pharmgkb | rs2228607 |
| gwascentral | rs2228607 |
| openSNP | rs2228607 |
| 23andMe | rs2228607 |
| SNPshot | rs2228607 |
| SNPdbe | rs2228607 |
| MSV3d | rs2228607 |
| GWAS Ctlg | rs2228607 |
| GMAF | 0.4894 |
| Max Magnitude | 0 |
[PMID 23572023
] Clinical and molecular characterization of the potential CF disease modifier syntaxin 1A
[PMID 18593506] Genetic and expression analyses reveal elevated expression of syntaxin 1A ( STX1A) in high functioning autism.
