Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 5
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 5
rs3846662 0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58 5
rs393152 0.851 0.160 17 45641777 non coding transcript exon variant A/G snv 0.18 0.29 5
rs241448 0.882 0.200 6 32828908 stop lost A/G snv 0.32 0.27 5
rs1160985 1.000 0.080 19 44900155 intron variant C/T snv 0.52 5
rs439401 0.851 0.200 19 44911194 non coding transcript exon variant T/C snv 0.68 4
rs6834555 0.882 0.200 4 10060702 regulatory region variant G/A snv 0.74 4
rs714873 0.882 0.200 4 10057994 upstream gene variant G/A snv 0.74 4
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 4
rs12721109 1.000 0.080 19 44943964 intron variant G/A snv 1.3E-02 4
rs769449 0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02 4
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 4
rs6499640
FTO
0.925 0.160 16 53735765 intron variant G/A snv 0.59 4
rs9268856 0.807 0.240 6 32461942 intron variant C/A;T snv 4
rs9268877 0.827 0.200 6 32463370 intron variant A/G;T snv 4
rs13180 0.851 0.160 15 78497146 synonymous variant C/T snv 0.54 0.51 4
rs688 0.742 0.400 19 11116926 synonymous variant C/T snv 0.39 0.34 4
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 4
rs7232 1.000 0.080 11 60173126 missense variant T/A snv 0.31 0.27 4
rs387976 1.000 0.080 19 44875803 intron variant A/C;T snv 4
rs4803763 1.000 0.080 19 44854034 intron variant G/A;C snv 4
rs8106922 1.000 0.080 19 44898409 intron variant A/G snv 0.36 4
rs1483121 1.000 0.080 11 48311808 downstream gene variant G/A snv 9.7E-02 3
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 3