Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057518827
rs1057518827
G 0.700 GeneticVariation CLINVAR

dbSNP: rs138119149
rs138119149
A 0.700 GeneticVariation CLINVAR

dbSNP: rs190521996
rs190521996
C 0.700 CausalMutation CLINVAR

dbSNP: rs483352822
rs483352822
G 0.700 CausalMutation CLINVAR

dbSNP: rs587777589
rs587777589
GC 0.700 CausalMutation CLINVAR

dbSNP: rs80338701
rs80338701
A 0.700 CausalMutation CLINVAR

dbSNP: rs886039806
rs886039806
G 0.700 GeneticVariation CLINVAR

dbSNP: rs3764880
rs3764880
0.010 GeneticVariation BEFREE TLR7 rs3853839-G (G vs. C: p = 0.0100) and TLR8 rs3764880-G (recessive model: p = 0.0173; additive model: p = 0.0161) were associated with pericardial effusion in females relative to healthy females. 24445780

2014

dbSNP: rs3853839
rs3853839
0.010 GeneticVariation BEFREE TLR7 rs3853839-G (G vs. C: p = 0.0100) and TLR8 rs3764880-G (recessive model: p = 0.0173; additive model: p = 0.0161) were associated with pericardial effusion in females relative to healthy females. 24445780

2014

dbSNP: rs780581250
rs780581250
0.010 GeneticVariation BEFREE However, patients carrying the mutation 548T-->C had less severe disease, e.g., no pericardial effusions, malnutrition, or clinical coagulation disturbances. 11409861

2001