rs104895080, MEFV

N. diseases: 3
Disease: Multiple Sclerosis ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
0.010 GeneticVariation BEFREE Concurrent TNFRSF1A R92Q and pyrin E230K mutations in a child with multiple sclerosis. 20876156 2010