Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs1799941 0.763 0.280 17 7630105 5 prime UTR variant G/A snv 0.18 11
rs2057482 0.701 0.440 14 61747130 3 prime UTR variant T/C snv 0.84 0.80 21
rs4986938 0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33 35
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1800947
CRP
0.683 0.440 1 159713648 splice region variant C/A;G;T snv 4.4E-05; 5.1E-02; 4.0E-06 28
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs35767 0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv 13
rs7799039 0.649 0.560 7 128238730 upstream gene variant G/A;C snv 33