|| common in complete genomics
|?|| (A;A) (A;G) (G;G) ||28|
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.
[PMID 19180230] Multiple independent genetic factors at NOS1AP modulate the QT interval in a multi-ethnic population.
[PMID 19643915] Genetic variation in NOS1AP is associated with sudden cardiac death: evidence from the Rotterdam Study.