Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587777589
rs587777589
GC 0.700 CausalMutation CLINVAR

dbSNP: rs138119149
rs138119149
A 0.700 GeneticVariation CLINVAR

dbSNP: rs756312947
rs756312947
0.010 GeneticVariation BEFREE Additionally, SLE patients with Thr/Thr187 and Ile/Thr187 genotypes were more likely to have pleural effusions (P = 0.038, OR 1.874 [95% CI 1.033-3.411]) and anti-SSA/Ro antibody production (P = 0.046, OR 2.221 [95% CI 1.013-4.897]). 17133600

2006

dbSNP: rs1178187217
rs1178187217
A 0.700 GeneticVariation CLINVAR

dbSNP: rs201943194
rs201943194
T 0.700 CausalMutation CLINVAR

dbSNP: rs121434569
rs121434569
0.010 GeneticVariation BEFREE T790M mutations disappeared from cancer cells in the p</span>leural effusion after a break from the treatment drug and cytotoxic agent administration. 30145590

2018

dbSNP: rs730882245
rs730882245
A 0.700 GeneticVariation CLINVAR

dbSNP: rs387907272
rs387907272
0.010 GeneticVariation BEFREE In conclusion, in this small case series we showed that MYD88 L265P mutation analysis could serve as a useful adjunct in distinguishing benign from lymphomatous PE in patients with LPL. 31556196

2019

dbSNP: rs1057518827
rs1057518827
G 0.700 GeneticVariation CLINVAR

dbSNP: rs190521996
rs190521996
C 0.700 CausalMutation CLINVAR

dbSNP: rs80338701
rs80338701
A 0.700 CausalMutation CLINVAR

dbSNP: rs121918460
rs121918460
G 0.700 CausalMutation CLINVAR

dbSNP: rs483352822
rs483352822
G 0.700 CausalMutation CLINVAR

dbSNP: rs672601334
rs672601334
C 0.700 CausalMutation CLINVAR