rs10125157
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10125157(A;A) |
| Make rs10125157(A;C) |
| Make rs10125157(C;C) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 9 |
| Position | 118580943 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10125157 |
| dbSNP (classic) | rs10125157 |
| ClinGen | rs10125157 |
| ebi | rs10125157 |
| HLI | rs10125157 |
| Exac | rs10125157 |
| Gnomad | rs10125157 |
| Varsome | rs10125157 |
| LitVar | rs10125157 |
| Map | rs10125157 |
| PheGenI | rs10125157 |
| Biobank | rs10125157 |
| 1000 genomes | rs10125157 |
| hgdp | rs10125157 |
| ensembl | rs10125157 |
| geneview | rs10125157 |
| scholar | rs10125157 |
| rs10125157 | |
| pharmgkb | rs10125157 |
| gwascentral | rs10125157 |
| openSNP | rs10125157 |
| 23andMe | rs10125157 |
| SNPshot | rs10125157 |
| SNPdbe | rs10125157 |
| MSV3d | rs10125157 |
| GWAS Ctlg | rs10125157 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
[PMID 26083723] Lack of association between arterial stiffness and genetic variants by genome-wide association scan
