Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs822395 0.776 0.240 3 186849018 intron variant C/A;G snv 10
rs822396 0.732 0.400 3 186849088 intron variant G/A snv 0.81 16
rs869109213 0.790 0.200 7 150997269 intron variant GGGGGTGAGGAAGTCTAGACCTGCTGCG/A delins 10
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs7923837 0.882 0.160 10 92722160 intergenic variant G/A;T snv 8
rs1041981 0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 25
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1044250 0.807 0.240 19 8371280 missense variant C/T snv 0.30 0.29 12
rs1050450 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1138272 0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs11556218 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 27
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1232898090 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188