rs530390117, FASLG

N. diseases: 3
Disease: Sicca Syndrome ×
Source: BEFREE ×
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Sicca Syndrome
CUI: C0086981
Disease: Sicca Syndrome
0.010 GeneticVariation BEFREE Direct sequencing revealed a heterozygous point mutation ( - 259T/C) in the FasL gene promoter region in one SS patient with EEG. 17966039 2007