rs10498345, None

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Coronary Artery Vasospasm
CUI: C0010073
Disease: Coronary Artery Vasospasm
0.810 GeneticVariation GWASCAT Haplotype analysis showed that haplotype H2, the only haplotype containing the protective A allele at SNP rs10498345, was most strongly associated with coronary spasm (permutation P value <1x10(-4)). 18075462 2007
Coronary Artery Vasospasm
CUI: C0010073
Disease: Coronary Artery Vasospasm
0.810 GeneticVariation GWASDB Haplotype analysis showed that haplotype H2, the only haplotype containing the protective A allele at SNP rs10498345, was most strongly associated with coronary spasm (permutation P value <1x10(-4)). 18075462 2007
Coronary Artery Vasospasm
CUI: C0010073
Disease: Coronary Artery Vasospasm
0.810 GeneticVariation BEFREE SNP rs10498345 was strongly associated with coronary spasm in Japanese women utilizing genome-wide SNP analysis. 18075462 2007