rs6022662
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6022662(C;C) |
| Make rs6022662(C;T) |
| Make rs6022662(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 20 |
| Position | 53688088 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6022662 |
| dbSNP (classic) | rs6022662 |
| ClinGen | rs6022662 |
| ebi | rs6022662 |
| HLI | rs6022662 |
| Exac | rs6022662 |
| Gnomad | rs6022662 |
| Varsome | rs6022662 |
| LitVar | rs6022662 |
| Map | rs6022662 |
| PheGenI | rs6022662 |
| Biobank | rs6022662 |
| 1000 genomes | rs6022662 |
| hgdp | rs6022662 |
| ensembl | rs6022662 |
| geneview | rs6022662 |
| scholar | rs6022662 |
| rs6022662 | |
| pharmgkb | rs6022662 |
| gwascentral | rs6022662 |
| openSNP | rs6022662 |
| 23andMe | rs6022662 |
| SNPshot | rs6022662 |
| SNPdbe | rs6022662 |
| MSV3d | rs6022662 |
| GWAS Ctlg | rs6022662 |
| GMAF | 0.2548 |
| Max Magnitude | 0 |
Please note that this SNP is NOT associated with vitamin B12 deficiency. The original article was printed with a typo. Here is the correction: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2683944/pdf/main.pdf. The correct SNP is rs602662.
