Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2205960
rs2205960
TNFSF4
0.020 GeneticVariation BEFREE Case-control comparisons revealed a significant association between susceptibility to SS</span>c and the minor alleles at SNPs rs1234314 (OR 1.20, 95% CI 1.04 to 1.4, p(FDR)=0.019), rs2205960 (OR 1.24, 95% CI 1.10 to 1.50, p(FDR)=0.019) and rs844648 (OR 1.16, 95% CI 1.01 to 1.30, p(FDR)=0.032). 19778912

2010
dbSNP: rs2205960
rs2205960
TNFSF4
0.020 GeneticVariation BEFREE We confirm TNFSF4 as an SSc susceptibility gene and rs2205960 as a putative causal variant with preferential association in the ACA+ SSc subphenotype. 22422496

2012