Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2266788
rs2266788
ZPR1 ; APOA5
CUI: C0948242
Disease: Nuchal bleb, familial
Nuchal bleb, familial 		0.010 GeneticVariation BEFREE The 1891T>C (rs2266788) SNP was in LD (r(2)=0.68) with -1131T>C and -3A>G, and the minor allele was more frequent in FCH than controls (0.42 vs. 0.19, P<0.001). 19732897

2010