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.