Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387907272
rs387907272
0.050 GeneticVariation BEFREE Clinicopathologic correlates of <i>MYD88</i> L265P mutation and programmed cell death (PD-1) pathway in primary central nervous system lymphoma. 31184237

2019

dbSNP: rs387907272
rs387907272
0.050 GeneticVariation BEFREE In a cohort of 23 PCNSL patients, L265P MYD88 mutations were examined in tumor-free BM mononuclear cells (MNC) in which the PCNSL tumors had L265P MYD88 mutations. 30353605

2019

dbSNP: rs387907272
rs387907272
0.050 GeneticVariation BEFREE The MyD88 L265P mutation predicted a poor prognosis in elderly PCNSL patients. 29258950

2018

dbSNP: rs387907272
rs387907272
0.050 GeneticVariation BEFREE To investigate how sensitively the MYD88 L265P mutation can be identified in cell-free DNA from PCNSL patients, we carried out droplet digital PCR (ddPCR) and targeted deep sequencing (TDS) in 14 consecutive PCNSL patients from whom paired tumor-derived DNA and cell-free DNA was available at diagnosis. 29151258

2018

dbSNP: rs387907272
rs387907272
0.050 GeneticVariation BEFREE Nine of these samples tested positive for MYD88 p.(L265P) (8 LPL and 1 PCNSL). 29210102

2018