rs11086243
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11086243(C;C) |
| Make rs11086243(C;T) |
| Make rs11086243(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 20 |
| Position | 48150492 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11086243 |
| dbSNP (classic) | rs11086243 |
| ClinGen | rs11086243 |
| ebi | rs11086243 |
| HLI | rs11086243 |
| Exac | rs11086243 |
| Gnomad | rs11086243 |
| Varsome | rs11086243 |
| LitVar | rs11086243 |
| Map | rs11086243 |
| PheGenI | rs11086243 |
| Biobank | rs11086243 |
| 1000 genomes | rs11086243 |
| hgdp | rs11086243 |
| ensembl | rs11086243 |
| geneview | rs11086243 |
| scholar | rs11086243 |
| rs11086243 | |
| pharmgkb | rs11086243 |
| gwascentral | rs11086243 |
| openSNP | rs11086243 |
| 23andMe | rs11086243 |
| SNPshot | rs11086243 |
| SNPdbe | rs11086243 |
| MSV3d | rs11086243 |
| GWAS Ctlg | rs11086243 |
| GMAF | 0.3733 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21441931] |
| Trait | |
| Title | Common variation in GPC5 is associated with acquired nephrotic syndrome |
| Risk Allele | T |
| P-val | 0.000003 |
| Odds Ratio | 1.3700 [1.20-1.57] |
