Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
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
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs2333227
MPO
0.752 0.320 17 58281401 upstream gene variant C/T snv 0.24 15
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs57095329 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 25
rs689466 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 33
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs7483 0.742 0.320 1 109737079 missense variant C/T snv 4.0E-06; 0.35 0.26 11
rs2231142 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56