Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1008949
rs1008949
LOC105379321 ; LOC105379322 ; LOC107986926
0.010 GeneticVariation BEFREE The distribution of rs1008949 genotypes, dominant model, recessive model, and allele frequency did not show a significant difference between patients with CAD and the control subjects in the Han and Uygur groups. 24886494

2014