rs9844666
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;G) | AMD association | |
| (G;G) | AMD association |
| Make rs9844666(A;A) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 136255374 |
| Gene | PCCB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9844666 |
| dbSNP (classic) | rs9844666 |
| ClinGen | rs9844666 |
| ebi | rs9844666 |
| HLI | rs9844666 |
| Exac | rs9844666 |
| Gnomad | rs9844666 |
| Varsome | rs9844666 |
| LitVar | rs9844666 |
| Map | rs9844666 |
| PheGenI | rs9844666 |
| Biobank | rs9844666 |
| 1000 genomes | rs9844666 |
| hgdp | rs9844666 |
| ensembl | rs9844666 |
| geneview | rs9844666 |
| scholar | rs9844666 |
| rs9844666 | |
| pharmgkb | rs9844666 |
| gwascentral | rs9844666 |
| openSNP | rs9844666 |
| 23andMe | rs9844666 |
| SNPshot | rs9844666 |
| SNPdbe | rs9844666 |
| MSV3d | rs9844666 |
| GWAS Ctlg | rs9844666 |
| GMAF | 0.09183 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20881960 ]
|
| Trait | Height |
| Title | Hundreds of variants clustered in genomic loci and biological pathways affect human height. |
| Risk Allele | A |
| P-val | 4E-9 |
| Odds Ratio | .02 [NR] unit decrease |
G allele associated with AMD [1]
