Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs868412274
rs868412274
IL18R1
0.010 GeneticVariation BEFREE The NLRP3 E311K mutation is associated with a heterogeneous clinical spectrum, which may expand the view on MWS presentation.The leading symptom was hearing loss. 22146561

2011