Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 43
rs1556425596 0.752 0.240 21 45989967 intron variant C/T snv 37
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 36
rs1043679457 0.752 0.400 5 60927745 intron variant C/A;G;T snv 33
rs2075650 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 25
rs780093 0.763 0.240 2 27519736 intron variant T/C snv 0.68 25
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 25
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 25
rs12203592 0.649 0.320 6 396321 intron variant C/T snv 0.10 23
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 23
rs10401969 0.776 0.240 19 19296909 intron variant T/C snv 0.10 23
rs79105258 12 111280427 intron variant C/A;T snv 23
rs1535 0.752 0.240 11 61830500 intron variant A/G snv 0.31 22
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 21
rs12579302 0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs597808 0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs72928038 0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs4506565 0.790 0.280 10 112996282 intron variant A/G;T snv 19
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 19
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 19
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 19
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 19
rs17696736 0.827 0.240 12 112049014 intron variant A/G snv 0.30 18
rs11066280 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 18
rs2187668 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 18