rs41318021
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs41318021(C;T) |
| Make rs41318021(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 13 |
| Position | 29514470 |
| Gene | SLC7A1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs41318021 |
| dbSNP (classic) | rs41318021 |
| ClinGen | rs41318021 |
| ebi | rs41318021 |
| HLI | rs41318021 |
| Exac | rs41318021 |
| Gnomad | rs41318021 |
| Varsome | rs41318021 |
| LitVar | rs41318021 |
| Map | rs41318021 |
| PheGenI | rs41318021 |
| Biobank | rs41318021 |
| 1000 genomes | rs41318021 |
| hgdp | rs41318021 |
| ensembl | rs41318021 |
| geneview | rs41318021 |
| scholar | rs41318021 |
| rs41318021 | |
| pharmgkb | rs41318021 |
| gwascentral | rs41318021 |
| openSNP | rs41318021 |
| 23andMe | rs41318021 |
| SNPshot | rs41318021 |
| SNPdbe | rs41318021 |
| MSV3d | rs41318021 |
| GWAS Ctlg | rs41318021 |
| GMAF | 0.03857 |
| Max Magnitude | 0 |
[PMID 19067360] endothelial dysfunction seen in hypertensive subjects. notable that the authors initiated their own dbsnp entry and cite the ss# in the abstract as well as relating to microRNA
[PMID 23841815
] Contribution of SLC7A1 genetic variant to hypertension, the TAMRISK study
