Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs5882 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs3135506 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 26
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs693 0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 24
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs2303790 0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 19
rs1800775 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 18
rs1042034 0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 15
rs2075291 0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06 15
rs6511720 0.790 0.120 19 11091630 intron variant G/T snv 0.12 15
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs3812316 0.763 0.240 7 73606007 missense variant C/G snv 0.10 9.4E-02 14
rs10846744 0.763 0.160 12 124827879 intron variant G/C snv 0.32 11
rs320
LPL
0.827 0.200 8 19961566 intron variant T/A;G snv 9
rs1367117 1.000 0.080 2 21041028 missense variant G/A snv 0.26 0.24 8
rs264
LPL
0.882 0.080 8 19955669 intron variant G/A snv 0.14 6
rs56131196 0.925 0.160 19 44919589 downstream gene variant G/A snv 0.18 6