Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs778653907
rs778653907
TNFRSF1A
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