rs2061634
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2061634(C;C) |
| Make rs2061634(C;G) |
| Make rs2061634(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 97343500 |
| Gene | CCDC180, LOC100499484-C9ORF174 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2061634 |
| dbSNP (classic) | rs2061634 |
| ClinGen | rs2061634 |
| ebi | rs2061634 |
| HLI | rs2061634 |
| Exac | rs2061634 |
| Gnomad | rs2061634 |
| Varsome | rs2061634 |
| LitVar | rs2061634 |
| Map | rs2061634 |
| PheGenI | rs2061634 |
| Biobank | rs2061634 |
| 1000 genomes | rs2061634 |
| hgdp | rs2061634 |
| ensembl | rs2061634 |
| geneview | rs2061634 |
| scholar | rs2061634 |
| rs2061634 | |
| pharmgkb | rs2061634 |
| gwascentral | rs2061634 |
| openSNP | rs2061634 |
| 23andMe | rs2061634 |
| SNPshot | rs2061634 |
| SNPdbe | rs2061634 |
| MSV3d | rs2061634 |
| GWAS Ctlg | rs2061634 |
| GMAF | 0.2479 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 19442274
] First genome-wide association study for this disorder, albeit of 152 patients, reports an association between this SNP (odds ratio 2.04, p = 4.2 x10e-5) and Behcet's disease.
