Gene: BRAF ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs113488022
rs113488022
BRAF
0.020 GeneticVariation BEFREE Further, mutation of BRAF V600E was observed in 12 (41.4%) FNMTCs and 29 (85.3%) NMTCs. 21826673

2012
dbSNP: rs113488022
rs113488022
BRAF
0.020 GeneticVariation BEFREE The T1799A BRAF mutation is not a germline mutation or susceptibility genetic event for FNMTC. 16117812

2005
dbSNP: rs121913377
rs121913377
BRAF
0.010 GeneticVariation BEFREE Further, mutation of BRAF V600E was observed in 12 (41.4%) FNMTCs and 29 (85.3%) NMTCs. 21826673

2012