Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121908147
rs121908147
NLRP3
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.010 GeneticVariation BEFREE The V198M mutation in the CIAS1 gene was identified in one patient with typical BD but no symptoms of CAPS. 17213252

2007