rs7757648
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common genotype |
| Make rs7757648(A;A) |
| Make rs7757648(A;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 6 |
| Position | 30884156 |
| Gene | DDR1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7757648 |
| dbSNP (classic) | rs7757648 |
| ClinGen | rs7757648 |
| ebi | rs7757648 |
| HLI | rs7757648 |
| Exac | rs7757648 |
| Gnomad | rs7757648 |
| Varsome | rs7757648 |
| LitVar | rs7757648 |
| Map | rs7757648 |
| PheGenI | rs7757648 |
| Biobank | rs7757648 |
| 1000 genomes | rs7757648 |
| hgdp | rs7757648 |
| ensembl | rs7757648 |
| geneview | rs7757648 |
| scholar | rs7757648 |
| rs7757648 | |
| pharmgkb | rs7757648 |
| gwascentral | rs7757648 |
| openSNP | rs7757648 |
| 23andMe | rs7757648 |
| SNPshot | rs7757648 |
| SNPdbe | rs7757648 |
| MSV3d | rs7757648 |
| GWAS Ctlg | rs7757648 |
| Max Magnitude | 0 |
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
