rs4634
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs4634(A;A) |
| Make rs4634(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 47292423 |
| Gene | ITGB3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4634 |
| dbSNP (classic) | rs4634 |
| ClinGen | rs4634 |
| ebi | rs4634 |
| HLI | rs4634 |
| Exac | rs4634 |
| Gnomad | rs4634 |
| Varsome | rs4634 |
| LitVar | rs4634 |
| Map | rs4634 |
| PheGenI | rs4634 |
| Biobank | rs4634 |
| 1000 genomes | rs4634 |
| hgdp | rs4634 |
| ensembl | rs4634 |
| geneview | rs4634 |
| scholar | rs4634 |
| rs4634 | |
| pharmgkb | rs4634 |
| gwascentral | rs4634 |
| openSNP | rs4634 |
| 23andMe | rs4634 |
| SNPshot | rs4634 |
| SNPdbe | rs4634 |
| MSV3d | rs4634 |
| GWAS Ctlg | rs4634 |
| GMAF | 0.2948 |
| Max Magnitude | 0 |
[PMID 22246292] Genetic and epigenetic mechanisms collaborate to control SERPINA3 expression and its association with placental diseases
| ClinVar | |
|---|---|
| Risk | rs4634(A;A) |
| Alt | rs4634(A;A) |
| Reference | Rs4634(G;G) |
| Significance | Non-pathogenic |
| Disease | not specified Glanzmann thrombasthenia |
| Variation | info |
| Gene | ITGB3 |
| CLNDBN | not specified Glanzmann thrombasthenia |
| Reversed | 0 |
| HGVS | NC_000017.10:g.45369789G>A |
| CLNSRC | |
| CLNACC | RCV000241947.1, RCV000394843.1, |
