rs699512
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs699512(A;A) |
| Make rs699512(A;G) |
| Make rs699512(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 43771165 |
| Gene | BLVRA, LOC102724946 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs699512 |
| dbSNP (classic) | rs699512 |
| ClinGen | rs699512 |
| ebi | rs699512 |
| HLI | rs699512 |
| Exac | rs699512 |
| Gnomad | rs699512 |
| Varsome | rs699512 |
| LitVar | rs699512 |
| Map | rs699512 |
| PheGenI | rs699512 |
| Biobank | rs699512 |
| 1000 genomes | rs699512 |
| hgdp | rs699512 |
| ensembl | rs699512 |
| geneview | rs699512 |
| scholar | rs699512 |
| rs699512 | |
| pharmgkb | rs699512 |
| gwascentral | rs699512 |
| openSNP | rs699512 |
| 23andMe | rs699512 |
| SNPshot | rs699512 |
| SNPdbe | rs699512 |
| MSV3d | rs699512 |
| GWAS Ctlg | rs699512 |
| GMAF | 0.2089 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 21721974] Association of a BLVRA Common Polymorphism with Essential Hypertension and Blood Pressure in Kazaks
[PMID 19284636
] Missing call bias in high-throughput genotyping.
[PMID 30636082] Associations between G6PD, OATP1B1 and BLVRA variants and susceptibility to neonatal hyperbilirubinaemia in a Chinese Han population.
