Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs2070744 0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs2430561 0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs1800587 0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs1800797 0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs5742909 0.614 0.680 2 203867624 upstream gene variant C/T snv 6.7E-02 40
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 33