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: rs121434569
rs121434569
0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.040 1.000 4 2016 2019
dbSNP: rs1057519847
rs1057519847
0.570 0.560 7 55191821 missense variant CT/AG mnv
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 1.000 1 2012 2012
dbSNP: rs1057519848
rs1057519848
0.570 0.560 7 55191822 missense variant TG/GT mnv
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 1.000 1 2012 2012
dbSNP: rs121434568
rs121434568
0.568 0.560 7 55191822 missense variant T/A;G snv
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 1.000 1 2012 2012
dbSNP: rs2227983
rs2227983
0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 < 0.001 1 2010 2010
dbSNP: rs961150162
rs961150162
7 55198779 missense variant G/A;C snv
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 1.000 1 2016 2016