rs12425791, None

N. diseases: 4
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Large-artery atherosclerosis (embolus/thrombosis)
CUI: C4699512
Disease: Large-artery atherosclerosis (embolus/thrombosis)
0.030 GeneticVariation BEFREE These findings indicated that rs12425791 and rs11833579 on chromosome 12p13 may be useful biomarkers for predicting the prognosis of patients with the LAA subtype of ischaemic stroke. 24995625 2014
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
0.010 GeneticVariation BEFREE Homozygosity of two NINJ2 SNPs was significantly associated with a decreased risk of AD [rs11833579: adjusted odds ratio (AOR) = 0.43; 95% confidence interval (CI)= 0.23-0.80; rs12425791: AOR= 0.33, 95% CI= 0.12-0.96]. 21674003 2011
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
0.890 GeneticVariation GWASDB Genomewide association studies of stroke. 19369658 2009
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
0.890 GeneticVariation GWASCAT Genomewide association studies of stroke. 19369658 2009