Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1129844 0.752 0.320 17 34285875 missense variant G/A;C;T snv 0.16; 1.2E-05 13
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs17235409 0.653 0.600 2 218395009 missense variant G/A;C snv 4.9E-02; 4.1E-06 31
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs222747 0.827 0.240 17 3589906 missense variant C/A;G;T snv 0.72; 4.5E-06 8
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs56149945 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 49
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs1258159645 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs1022113606 0.732 0.280 4 24800161 missense variant G/C snv 1.6E-04 2.1E-05 17
rs76863441 0.672 0.440 6 46709361 missense variant C/A snv 4.5E-03 1.3E-03 25