Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1033069
rs1033069
1.000 0.040 2 213900484 intron variant A/G snv 0.58
CUI: C4725671
Disease: High-Risk Neuroblastoma
High-Risk Neuroblastoma
0.010 1.000 1 2013 2013
dbSNP: rs11103603
rs11103603
0.851 0.080 9 134449754 TF binding site variant T/C snv 0.46
CUI: C4725671
Disease: High-Risk Neuroblastoma
High-Risk Neuroblastoma
0.010 1.000 1 2019 2019
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C4725671
Disease: High-Risk Neuroblastoma
High-Risk Neuroblastoma
0.010 1.000 1 2009 2009
dbSNP: rs6776706
rs6776706
0.851 0.080 3 25439731 intron variant T/A snv 0.27
CUI: C4725671
Disease: High-Risk Neuroblastoma
High-Risk Neuroblastoma
0.010 1.000 1 2019 2019