Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs6280 0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs2236225 0.614 0.640 14 64442127 missense variant G/A snv 0.44 0.38 52
rs6318 0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs53576 0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs6311 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs121909224 0.627 0.560 10 87933147 stop gained C/G;T snv 1.2E-05 41
rs1051266 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs149617956 0.672 0.560 3 69964940 missense variant G/A snv 1.4E-03 1.6E-03 32
rs1360780 0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs1801260 0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs104894396 0.672 0.400 13 20189511 stop gained C/T snv 5.8E-04 1.1E-04 28
rs137854539 0.716 0.520 20 58903703 missense variant C/T snv 28