rs7977109
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7977109(A;A) |
| Make rs7977109(A;G) |
| Make rs7977109(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 117292535 |
| Gene | NOS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7977109 |
| dbSNP (classic) | rs7977109 |
| ClinGen | rs7977109 |
| ebi | rs7977109 |
| HLI | rs7977109 |
| Exac | rs7977109 |
| Gnomad | rs7977109 |
| Varsome | rs7977109 |
| LitVar | rs7977109 |
| Map | rs7977109 |
| PheGenI | rs7977109 |
| Biobank | rs7977109 |
| 1000 genomes | rs7977109 |
| hgdp | rs7977109 |
| ensembl | rs7977109 |
| geneview | rs7977109 |
| scholar | rs7977109 |
| rs7977109 | |
| pharmgkb | rs7977109 |
| gwascentral | rs7977109 |
| openSNP | rs7977109 |
| 23andMe | rs7977109 |
| SNPshot | rs7977109 |
| SNPdbe | rs7977109 |
| MSV3d | rs7977109 |
| GWAS Ctlg | rs7977109 |
| GMAF | 0.3641 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
After scanning a region of chromosome 12 previously linked to restless legs syndrome in ~900 patients, German investigators found SNPs within the NOS1 gene to be most associated with the syndrome. SNP rs7977109 yielded an odds ratio of 0.76 (CI: 0.64 -0.90, p=-.002). The risk allele is said to be defined in Supplementary materials available online, but they aren't. Furthermore, the significant association seen for this SNP and one other (rs693534) are in opposite directions in the explorative versus the replication populations.[PMID 18058820]
[PMID 20401335
] Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.
