rs16840639
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs16840639(C;C) |
| Make rs16840639(C;T) |
| Make rs16840639(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 196855643 |
| Gene | LOC100289145 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs16840639 |
| dbSNP (classic) | rs16840639 |
| ClinGen | rs16840639 |
| ebi | rs16840639 |
| HLI | rs16840639 |
| Exac | rs16840639 |
| Gnomad | rs16840639 |
| Varsome | rs16840639 |
| LitVar | rs16840639 |
| Map | rs16840639 |
| PheGenI | rs16840639 |
| Biobank | rs16840639 |
| 1000 genomes | rs16840639 |
| hgdp | rs16840639 |
| ensembl | rs16840639 |
| geneview | rs16840639 |
| scholar | rs16840639 |
| rs16840639 | |
| pharmgkb | rs16840639 |
| gwascentral | rs16840639 |
| openSNP | rs16840639 |
| 23andMe | rs16840639 |
| SNPshot | rs16840639 |
| SNPdbe | rs16840639 |
| MSV3d | rs16840639 |
| GWAS Ctlg | rs16840639 |
| GMAF | 0.1887 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19789632
] We found that YRI have significantly lower copy number of CFHR3 gene (Complement Factor H-Related gene 3) than CEU and ASN individuals. In addition, we have observed that this variant is well tagged by a SNP (rs16840639; r2 = 0.79)
[PMID 21637784] Association of genetic variants in complement factor h and factor h-related genes with systemic lupus erythematosus susceptibility
[PMID 23582991] Genetic Influences on the Outcome of Anti-Vascular Endothelial Growth Factor Treatment in Neovascular Age-related Macular Degeneration
