rs16946160
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs16946160(A;A) |
| Make rs16946160(A;G) |
| Make rs16946160(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 13 |
| Position | 91551559 |
| Gene | GPC5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs16946160 |
| dbSNP (classic) | rs16946160 |
| ClinGen | rs16946160 |
| ebi | rs16946160 |
| HLI | rs16946160 |
| Exac | rs16946160 |
| Gnomad | rs16946160 |
| Varsome | rs16946160 |
| LitVar | rs16946160 |
| Map | rs16946160 |
| PheGenI | rs16946160 |
| Biobank | rs16946160 |
| 1000 genomes | rs16946160 |
| hgdp | rs16946160 |
| ensembl | rs16946160 |
| geneview | rs16946160 |
| scholar | rs16946160 |
| rs16946160 | |
| pharmgkb | rs16946160 |
| gwascentral | rs16946160 |
| openSNP | rs16946160 |
| 23andMe | rs16946160 |
| SNPshot | rs16946160 |
| SNPdbe | rs16946160 |
| MSV3d | rs16946160 |
| GWAS Ctlg | rs16946160 |
| GMAF | 0.1607 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21441931] |
| Trait | |
| Title | Common variation in GPC5 is associated with acquired nephrotic syndrome |
| Risk Allele | A |
| P-val | 3E-7 |
| Odds Ratio | 1.3900 [1.22-1.57] |
