rs662799, APOA5

N. diseases: 33
Disease: Nuchal bleb, familial ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Nuchal bleb, familial
CUI: C0948242
Disease: Nuchal bleb, familial
0.010 GeneticVariation BEFREE The -1131T>C (rs662799) and -3A>G (rs651821) SNPs in APOA5 were in almost complete linkage disequilibrium (LD, r(2)=0.99), and their minor alleles were more frequent (P<0.001) in FCH than controls (0.60 vs. 0.24). 19732897 2010