Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10010131 0.827 0.120 4 6291188 intron variant A/G snv 0.66 0.63 7
rs1058046
PYY
0.925 0.120 17 43953163 missense variant G/C snv 0.63 0.59 2
rs10885406 0.925 0.120 10 113017965 intron variant A/G snv 0.55 2
rs10968576 0.882 0.120 9 28414341 intron variant A/G snv 0.26 10
rs11075989
FTO
0.925 0.120 16 53785965 intron variant C/A;T snv 3
rs11075990
FTO
0.925 0.120 16 53785981 intron variant A/G snv 0.41 6
rs11076023
FTO
0.925 0.120 16 54118136 3 prime UTR variant A/T snv 0.49 2
rs11642015
FTO
0.925 0.120 16 53768582 intron variant C/T snv 0.31 9
rs11642841
FTO
0.925 0.120 16 53811575 intron variant C/A;G snv 3
rs116454156 0.925 0.120 10 93587284 missense variant G/A snv 1.8E-02 1.4E-02 3
rs11671664 0.925 0.120 19 45669020 intron variant G/A snv 0.12 5
rs11960429 0.925 0.120 5 180739677 missense variant G/A snv 1.2E-02 1.5E-02 2
rs12104705 0.882 0.120 2 162435107 intron variant C/T snv 0.15 4
rs12156368 0.925 0.120 8 18885203 intron variant C/T snv 0.36 2
rs13078807 0.925 0.120 3 85835000 intron variant A/G snv 0.15 5
rs1412239 0.925 0.120 9 28425517 intron variant C/G snv 0.26 4
rs150016118 0.882 0.120 11 74006339 missense variant A/G snv 1.7E-05 6.3E-05 6
rs1541276 0.925 0.120 18 13825728 splice region variant A/C snv 0.17 0.19 2
rs1550805 0.925 0.120 5 68287979 intron variant C/T snv 6.9E-02 2
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 21
rs16861194 0.925 0.120 3 186841636 upstream gene variant A/G snv 0.15 2
rs17700633 0.882 0.120 18 60262199 intergenic variant G/A snv 0.28 4
rs17817964
FTO
0.925 0.120 16 53794154 intron variant C/T snv 0.30 6
rs1797 0.925 0.120 10 117945927 intergenic variant C/T snv 0.45 2
rs1805081 0.925 0.120 18 23560468 missense variant T/C snv 0.33 0.29 3