Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12495941 0.851 0.280 3 186850391 intron variant G/T snv 0.35 5
rs1271572 0.708 0.400 14 64295199 intron variant A/C;T snv 16
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs16147 0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48 18
rs17366568 0.851 0.200 3 186852664 non coding transcript exon variant G/A snv 8.8E-02 6
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs182052 0.701 0.440 3 186842993 intron variant G/A snv 0.38 19
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs243865 0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs2794521
CRP
0.742 0.480 1 159715306 upstream gene variant C/T snv 0.78 15
rs3774261 0.776 0.320 3 186853770 splice region variant A/G snv 0.55 10
rs3918242 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs599839 0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs670 0.763 0.360 11 116837697 5 prime UTR variant C/T snv 0.17 13
rs6782181 0.851 0.160 3 138386212 intron variant G/A;C snv 6
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 17
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs822396 0.732 0.400 3 186849088 intron variant G/A snv 0.81 16
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614