rs1321172
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | common | |
| (C;G) | 1.08x risk | |
| (G;G) | >1.08x risk |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 66265030 |
| Gene | PDE4B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1321172 |
| dbSNP (classic) | rs1321172 |
| ClinGen | rs1321172 |
| ebi | rs1321172 |
| HLI | rs1321172 |
| Exac | rs1321172 |
| Gnomad | rs1321172 |
| Varsome | rs1321172 |
| LitVar | rs1321172 |
| Map | rs1321172 |
| PheGenI | rs1321172 |
| Biobank | rs1321172 |
| 1000 genomes | rs1321172 |
| hgdp | rs1321172 |
| ensembl | rs1321172 |
| geneview | rs1321172 |
| scholar | rs1321172 |
| rs1321172 | |
| pharmgkb | rs1321172 |
| gwascentral | rs1321172 |
| openSNP | rs1321172 |
| 23andMe | rs1321172 |
| SNPshot | rs1321172 |
| SNPdbe | rs1321172 |
| MSV3d | rs1321172 |
| GWAS Ctlg | rs1321172 |
| GMAF | 0.3269 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
rs1321172 has been reported in a large study to be associated with multiple sclerosis.
The risk allele (oriented to the dbSNP entry) is (G); the odds ratio associated with this allele is 1.08 (CI 1.02-1.14). [PMID 17660530]
[PMID 22492128] Association of SNPs rs6498169 and rs10984447 with multiple sclerosis in Saudi patients: a model of the usefulness of familial aggregates in identifying genetic linkage in a multifactorial disease.
