Rs12567209
From SNPedia
| is a | snp |
| is | mentioned by |
| dbSNP | rs12567209 |
| hapmap | rs12567209 |
| hgdp | rs12567209 |
| ensembl | rs12567209 |
| gopubmed | rs12567209 |
| scholar | rs12567209 |
| rs12567209 | |
| pharmgkb | rs12567209 |
| hgvbaseg2p | rs12567209 |
| medrefsnp | rs12567209 |
| 23andMe | rs12567209 |
| SNP Nexus |
| Chromosome | 1 |
| Orientation | plus |
| Position | 160303102 |
| Genotype | Effect |
|---|---|
| rs12567209(A;A)* | ? |
| rs12567209(A;G)* | ? |
| rs12567209(G;G)* | ? |
[PMID 19204306] rs10494366, rs4657139 and rs16847548 were significantly associated with adjusted QT interval in whites. relative hazard of SCD associated with each C allele at rs16847548 was 1.31. rs12567209 was also independently associated with SCD in whites (relative hazard 0.57, 95% confidence interval 0.39 to 0.83, P=0.003). No significant associations observed in blacks.
| ? | (A;A) (A;G) (G;G) |
|---|---|
|
| |
