Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs3918242 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs61750420 0.689 0.480 7 92501562 missense variant C/T snv 3.2E-04 3.5E-04 52
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs243865 0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs10889677 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs28929474 0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 37
rs187084 0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33