rs2044859
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 1 | Migraine |
| Make rs2044859(C;C) |
| Make rs2044859(C;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 7 |
| Position | 50544864 |
| Gene | DDC |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2044859 |
| dbSNP (classic) | rs2044859 |
| ClinGen | rs2044859 |
| ebi | rs2044859 |
| HLI | rs2044859 |
| Exac | rs2044859 |
| Gnomad | rs2044859 |
| Varsome | rs2044859 |
| LitVar | rs2044859 |
| Map | rs2044859 |
| PheGenI | rs2044859 |
| Biobank | rs2044859 |
| 1000 genomes | rs2044859 |
| hgdp | rs2044859 |
| ensembl | rs2044859 |
| geneview | rs2044859 |
| scholar | rs2044859 |
| rs2044859 | |
| pharmgkb | rs2044859 |
| gwascentral | rs2044859 |
| openSNP | rs2044859 |
| 23andMe | rs2044859 |
| SNPshot | rs2044859 |
| SNPdbe | rs2044859 |
| MSV3d | rs2044859 |
| GWAS Ctlg | rs2044859 |
| GMAF | 0.3838 |
| Max Magnitude | 1 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19455600] a haplotype consisting of rs2329340(A), rs11974297(C), rs2044859(T) and rs11761683(G) associated with increased incidence of migraine with aura among a sample of 528 migraine patients (308 without aura, 220 with aura) and 528 sex-matched migraine-free controls
[PMID 22397633] Neurotransmitter systems and neurotrophic factors in autism: association study of 37 genes suggests involvement of DDC.
