rs6658835
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6658835(A;A) |
| Make rs6658835(A;G) |
| Make rs6658835(G;G) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 1 |
| Position | 218347653 |
| Gene | TGFB2, TGFB2-AS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6658835 |
| dbSNP (classic) | rs6658835 |
| ClinGen | rs6658835 |
| ebi | rs6658835 |
| HLI | rs6658835 |
| Exac | rs6658835 |
| Gnomad | rs6658835 |
| Varsome | rs6658835 |
| LitVar | rs6658835 |
| Map | rs6658835 |
| PheGenI | rs6658835 |
| Biobank | rs6658835 |
| 1000 genomes | rs6658835 |
| hgdp | rs6658835 |
| ensembl | rs6658835 |
| geneview | rs6658835 |
| scholar | rs6658835 |
| rs6658835 | |
| pharmgkb | rs6658835 |
| gwascentral | rs6658835 |
| openSNP | rs6658835 |
| 23andMe | rs6658835 |
| SNPshot | rs6658835 |
| SNPdbe | rs6658835 |
| MSV3d | rs6658835 |
| GWAS Ctlg | rs6658835 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 27564654] Genetic variance of transforming growth factor β2 gene in conotruncal heart defects.
