MEFV, MEFV innate immuity regulator, pyrin, 4210

N. diseases: 410; N. variants: 72
Disease: Behcet Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104895094
rs104895094
Entrez Id: 4210
Gene Symbol: MEFV
MEFV
CUI: C0004943
Disease:
Behcet Syndrome 		0.010 GeneticVariation BEFREE The heterozygous MEFV mutation (K695R) was found in one (2%) BD patient. 16273767 2006