Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800206 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs4803750 0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs746682028 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs2279590
CLU
0.851 0.200 8 27598736 non coding transcript exon variant T/C snv 0.69 5
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41