Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057519864
rs1057519864
AR
0.010 GeneticVariation BEFREE The consequence of suppressing AR-F876L may then abrogate AR-F876L mediated CRPC cell proliferation and metastasis. 27233475

2016

dbSNP: rs1340026226
rs1340026226
AR
0.010 GeneticVariation BEFREE Selection was evident for the promiscuous receptor AR-V716M, which dominated three metastases from one flutamide-treated patient. 19366804

2009

dbSNP: rs137852578
rs137852578
AR
0.010 GeneticVariation BEFREE The cortisol/cortisone-responsive AR (AR(ccr)) has two mutations (L701H and T877A) that were found in the MDA PCa human prostate cancer cell lines established from a castrated patient whose metastatic tumor exhibited androgen-independent growth. 11956172

2002

dbSNP: rs864622007
rs864622007
AR
0.010 GeneticVariation BEFREE The cortisol/cortisone-responsive AR (AR(ccr)) has two mutations (L701H and T877A) that were found in the MDA PCa human prostate cancer cell lines established from a castrated patient whose metastatic tumor exhibited androgen-independent growth. 11956172

2002

dbSNP: rs976306779
rs976306779
AR
0.010 GeneticVariation BEFREE The influence of S100P on tumor growth and metastases were assessed in vivo. 18452169

2008

dbSNP: rs1052667
rs1052667
0.010 GeneticVariation BEFREE Moreover, rs1052667 polymorphism was correlated with such pathological features of osteosarcoma as tumor size, tumor grade, and tumor metastasis. 25136583

2014

dbSNP: rs1040411
rs1040411
0.010 GeneticVariation BEFREE Recent GWAS study identified rs4946728 and rs1040411 noncoding SNPs located between PRDM1 and ATG1 genes on chromosome 6q21 as risk factors for secondary malignancies in patients formerly treated with radiotherapy for pediatric Hodgkin disease. 24306881

2014

dbSNP: rs3804329
rs3804329
0.010 GeneticVariation BEFREE Both rs1322178 and rs3804329 can predict early distant metastasis of patients. 29207660

2017

dbSNP: rs4946728
rs4946728
0.010 GeneticVariation BEFREE Recent GWAS study identified rs4946728 and rs1040411 noncoding SNPs located between PRDM1 and ATG1 genes on chromosome 6q21 as risk factors for secondary malignancies in patients formerly treated with radiotherapy for pediatric Hodgkin disease. 24306881

2014

dbSNP: rs2064863
rs2064863
0.010 GeneticVariation BEFREE Moreover, patients with rs2064863 G allele exhibited a slightly lower risk of lymph node metastasis and those with rs6024836 G allele exhibited a lower risk of distant metastases. 31031846

2019

dbSNP: rs6024836
rs6024836
0.010 GeneticVariation BEFREE Moreover, patients with rs2064863 G allele exhibited a slightly lower risk of lymph node metastasis and those with rs6024836 G allele exhibited a lower risk of distant metastases. 31031846

2019

dbSNP: rs4671393
rs4671393
0.010 GeneticVariation BEFREE Moreover, the OR of lymph node metastasis patients at rs4671393 G alleles was 2.41 (P < 0.01); it was 1.38 (P = 0.035) in patients without lymph metastasis. 28225775

2017

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE However, there was no significant association between BRAF(V600E) mutation and factors including age > 45 (OR = 0.98; 95%CI = 0.89-1.07), tumor size (OR = 0.84; 95%CI = 0.64-1.09) and distant metastasis (OR = 1.23; 95%CI = 0.67-2.27). 26871894

2016

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE None of the 30 metastases and 10 primary uveal melanomas tested expressed the V599E mutation. 14522889

2003

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE BRAF(V599E) tended to be associated, although not significantly, with a greater volume and extension of the tumour and with lymph-nodal metastases at surgery. 15272920

2004

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE At univariate analysis the worst outcome for PTC patients was significantly correlated with clinicopathological features (i.e. age, tumor size, extrathyroid extension, lymph node and distant metastases, advanced stage, vascular endothelial growth factor expression, and vascular invasion) and the BRAF(V600E) mutation (P < 0.002). 18682506

2008

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE Interestingly, cells carrying the BRAF(V600E) mutation were not only found among cells surrounding the primary tumor but were also present in the stroma of melanoma metastases as well as in a histologically tumor-free re-excision sample from a patient who subsequently developed a local recurrence. 27338362

2016

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE Associations between BRAF V600E and TERT promoter mutations and clinicopathological features, Tumor-Node-Metastasis stage, initial risk, response to therapy, follow-up, and final disease outcome were assessed according to American Thyroid Association 2015 criteria and the American Joint Committee on Cancer/Tumor-Node-Metastasis (8th edition) staging system.Median follow-up was 120 months. 31305897

2019

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE The TERT promoter mutation is an independent predictor for distant metastasis of WDTC, but ALK testing is not useful for clinical decision-making in Korean patients with a high prevalence of the BRAF V600E mutation. 26857243

2016

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE Unexpectedly, V599 and V599E mutations were absent in cutaneous/subcutaneous metastases derived from acrolentiginous melanomas as preceding primary tumours. 15935100

2005

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE The BRAF(V600E) mutation was detected in 88 of the tumors examined, with significant differences between groups with and without lymph node (LN) metastases; the mean age of patients with BRAF(V600E) mutation was significantly higher than that of patients without mutations. 17685465

2007

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE NRAS mutant/BRAF wild type metastatic deposits were identified in three patients, with one patient having a BRAF V600E mutant metastatic tumour. 31023480

2019

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE BRAF(V600E) was characterized in 113 PTC patients diagnosed with pT1aNo-x (one PTC focus with a diameter <1 cm, without lymph node or distant metastases according to IUCC/AJCC TNM staging system 2010). 24354346

2014

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE All patients with lateral cervical node metastasis (n=9), and all but one tumor with extrathyroidal extension (n=17/18) showed BRAF(V600E) mutation. 22918165

2013

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE There were significant differences in clinicopathological parameters, such as extrathyroidal extension (P=0.031), nodal metastasis (P=0.021) and BRAF(V600E) mutation (P=0.039), between NF-κB-positive and negative PTCs. 23528368

2013