Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104895297
rs104895297
MVK
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 GeneticVariation BEFREE Two patients had paired mutations in the MVK gene (genotypes V377I/V377I and V377I/S135L) and displayed typical features of BD and MKD. 17213252

2007