Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7561317 0.925 0.120 2 644953 intergenic variant A/G snv 0.81 4
rs8089364 0.925 0.120 18 60191596 upstream gene variant T/C snv 0.21 4
rs998584 6 43790159 downstream gene variant C/A snv 0.41 4
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 4
rs11603334
ARAP1
1.000 0.080 11 72721940 5 prime UTR variant G/A snv 0.12 4
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 4
rs925946
BDNF-AS
0.882 0.120 11 27645655 intron variant T/G snv 0.72 4
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 4
rs12149832
FTO
0.851 0.120 16 53808996 intron variant G/A snv 0.31 4
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 4
rs3751812
FTO
0.882 0.160 16 53784548 intron variant G/T snv 0.30 4
rs6499640
FTO
0.925 0.160 16 53735765 intron variant G/A snv 0.59 4
rs7193144
FTO
0.925 0.120 16 53776774 intron variant T/C snv 0.40 4
rs9941349
FTO
1.000 0.080 16 53791576 intron variant C/T snv 0.34 4
rs2237892
KCNQ1
0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 4
rs2815752
LOC105378797
0.925 0.200 1 72346757 intron variant G/A snv 0.62 4
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 4
rs7200543
PDXDC1
16 15036113 synonymous variant A/G snv 0.35 0.30 4
rs340874
PROX1 ; PROX1-AS1
0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40 4
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 4
rs10885122 1.000 0.080 10 111282335 intergenic variant T/G snv 0.71 3
rs11084753 1.000 0.080 19 33831232 intergenic variant A/C;G;T snv 0.65 3
rs11257655 1.000 0.080 10 12265895 TF binding site variant C/T snv 0.23 3
rs12463617 1.000 0.080 2 629244 regulatory region variant A/C;T snv 3
rs12967135 18 60181790 intergenic variant G/A snv 0.24 3