Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2061634
rs2061634
SUGT1P4-STRA6LP-CCDC180 ; CCDC180
0.010 GeneticVariation BEFREE Among the associated SNPs, the Behçet's disease-risk allele in rs2061634 leads to substitution of serine to cysteine at amino acid position 995 (S995C) in the KIAA1529 protein. 19442274

2009