Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1800693
rs1800693
TNFRSF1A
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		C 0.880 GeneticVariation GWASCAT Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation. 27386562

2016
dbSNP: rs1800693
rs1800693
TNFRSF1A
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		G 0.880 GeneticVariation GWASCAT Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis. 24076602

2013
dbSNP: rs1800693
rs1800693
TNFRSF1A
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		G 0.880 GeneticVariation GWASCAT Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 21833088

2011
dbSNP: rs1800693
rs1800693
TNFRSF1A
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		C 0.880 GeneticVariation GWASCAT Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci. 19525953

2009