Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs879253942
rs879253942
TP53
0.010 GeneticVariation BEFREE The MYD88 L265P mutation is present in nearly 90% of patients with Waldenström macroglobulinemia. 30190015

2018