rs7148590
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7148590(A;A) |
| Make rs7148590(A;G) |
| Make rs7148590(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 14 |
| Position | 65006478 |
| Gene | CHURC1-FNTB, FNTB, MAX |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7148590 |
| dbSNP (classic) | rs7148590 |
| ClinGen | rs7148590 |
| ebi | rs7148590 |
| HLI | rs7148590 |
| Exac | rs7148590 |
| Gnomad | rs7148590 |
| Varsome | rs7148590 |
| LitVar | rs7148590 |
| Map | rs7148590 |
| PheGenI | rs7148590 |
| Biobank | rs7148590 |
| 1000 genomes | rs7148590 |
| hgdp | rs7148590 |
| ensembl | rs7148590 |
| geneview | rs7148590 |
| scholar | rs7148590 |
| rs7148590 | |
| pharmgkb | rs7148590 |
| gwascentral | rs7148590 |
| openSNP | rs7148590 |
| 23andMe | rs7148590 |
| SNPshot | rs7148590 |
| SNPdbe | rs7148590 |
| MSV3d | rs7148590 |
| GWAS Ctlg | rs7148590 |
| GMAF | 0.4353 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23720494 ]
|
| Trait | Blood trace element (Zn levels) |
| Title | Genome-wide association study identifies loci affecting blood copper, selenium and zinc. |
| Risk Allele | |
| P-val | 1E-7 |
| Odds Ratio | .14 [0.089-0.191] unit increase |
