Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2231142 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs759412116 0.581 0.640 19 45352210 missense variant C/G;T snv 4.0E-06; 6.0E-05 55
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs2236225 0.614 0.640 14 64442127 missense variant G/A snv 0.44 0.38 52
rs953038635 0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs2430561 0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs243865 0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs1800471 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 48
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47