Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3768716
rs3768716
0.820 GeneticVariation BEFREE After adjusted gender and age, seven out of eleven SNPs in <i>BARD1</i> were significant associated with the risk of NB, including one SNP in 5'-UTR (rs17489363 G > A), two SNPs in exon (rs2229571 G > C and rs3738888 C > T), and four SNPs in intron (rs3768716 A > G, rs6435862 T > G, rs3768707 C > T and rs17487792 C > T). 31258718

2019

dbSNP: rs3768716
rs3768716
0.820 GeneticVariation BEFREE Our results suggest that the BARD1 rs6435862 T>G and rs3768716 A>G polymorphisms may contribute to increased susceptibility to neuroblastoma, especially for the subjects at age ≥12 months, with adrenal gland-originated or with late clinical stage neuroblastoma. 26941572

2016

dbSNP: rs3768716
rs3768716
C 0.820 GeneticVariation GWASCAT Integrative genomics identifies LMO1 as a neuroblastoma oncogene. 21124317

2011

dbSNP: rs3768716
rs3768716
C 0.820 GeneticVariation GWASDB Integrative genomics identifies LMO1 as a neuroblastoma oncogene. 21124317

2011

dbSNP: rs3768716
rs3768716
0.820 GeneticVariation GWASDB We also tested the two most significant SNPs (rs6435862, rs3768716) in two additional independent high-risk neuroblastoma case series, yielding combined allelic odds ratios of 1.68 each (P = 8.65 x 10(-18) and 2.74 x 10(-16), respectively). 19412175

2009