Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs900400
LINC02029
0.925 0.080 3 157080986 upstream gene variant T/C snv 0.36 7
rs8043757
FTO
0.925 0.120 16 53779538 intron variant A/T snv 0.40 5
rs1320561 20 23117243 intergenic variant G/A snv 0.51 2
rs7822058
LOC105375835
8 52772301 intergenic variant T/C snv 0.89 2
rs6738627
SNORA70F ; COBLL1
2 164687940 intron variant G/A snv 0.44 2
rs11158559
SPTB
14 64774231 intron variant C/G;T snv 2
rs6071166 20 38704369 intergenic variant C/A snv 0.59 1
rs169082
DOCK2
5 169647052 intron variant C/T snv 0.45 1