rs8177441
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs8177441(C;C) |
| Make rs8177441(C;G) |
| Make rs8177441(G;G) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 5 |
| Position | 151026433 |
| Gene | GPX3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs8177441 |
| dbSNP (classic) | rs8177441 |
| ClinGen | rs8177441 |
| ebi | rs8177441 |
| HLI | rs8177441 |
| Exac | rs8177441 |
| Gnomad | rs8177441 |
| Varsome | rs8177441 |
| LitVar | rs8177441 |
| Map | rs8177441 |
| PheGenI | rs8177441 |
| Biobank | rs8177441 |
| 1000 genomes | rs8177441 |
| hgdp | rs8177441 |
| ensembl | rs8177441 |
| geneview | rs8177441 |
| scholar | rs8177441 |
| rs8177441 | |
| pharmgkb | rs8177441 |
| gwascentral | rs8177441 |
| openSNP | rs8177441 |
| 23andMe | rs8177441 |
| SNPshot | rs8177441 |
| SNPdbe | rs8177441 |
| MSV3d | rs8177441 |
| GWAS Ctlg | rs8177441 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 26612412
] A Three-Way Interaction among Maternal and Fetal Variants Contributing to Congenital Heart Defects.
