Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 18
rs6570507
ADGRG6
0.827 0.240 6 142358435 intron variant G/A snv 0.47 13
rs739496
SH2B3 ; ATXN2
0.790 0.160 12 111449855 3 prime UTR variant A/G snv 0.27 10
rs11205303
MTMR11
0.882 0.120 1 149934520 missense variant T/C snv 0.33 0.29 9
rs12149832
FTO
0.851 0.120 16 53808996 intron variant G/A snv 0.31 8
rs10052657
PDE4D
0.807 0.120 5 59111944 intron variant C/A snv 0.17 7
rs11157436
TRAV30
0.851 0.040 14 22168978 synonymous variant C/T snv 0.19 7
rs11190870 0.827 0.200 10 101219450 intergenic variant T/A;C snv 6
rs7741741
ADGRG6
0.925 0.040 6 142334664 intron variant T/A;G snv 6
rs6137473 0.827 0.280 20 21904055 intergenic variant G/A snv 0.61 5
rs10489629
IL23R ; C1orf141
0.827 0.240 1 67222666 intron variant T/C snv 0.48 5
rs12946942 0.882 0.200 17 71240857 intergenic variant G/T snv 7.5E-02 4
rs2384506 0.851 0.080 12 114991548 intergenic variant T/C snv 0.21 4
rs9389985
ADGRG6
0.925 0.040 6 142332761 intron variant A/G snv 0.40 4
rs17036090
ARHGEF38
0.925 0.040 4 105672417 intron variant T/C snv 5.0E-02 4
rs545608
CRYZL2P-SEC16B ; SEC16B
0.925 0.040 1 177929986 intron variant G/C snv 0.20 4
rs2254958
EIF2AK2
0.882 0.120 2 37149148 5 prime UTR variant G/A snv 0.34 4
rs678741
LBX1-AS1
0.851 0.200 10 101237824 intron variant G/A snv 0.51 4
rs2816992
NR5A2 ; LOC107985244
0.925 0.040 1 200100088 intron variant A/G snv 0.39 4
rs2764627
STARD13 ; STARD13-AS
0.925 0.040 13 33202941 intron variant C/T snv 5.0E-02 4
rs1254900
VAMP5
0.851 0.120 2 85589211 intron variant A/G snv 0.81 4
rs1086603 0.882 0.120 1 147816164 intergenic variant G/A snv 3.4E-02 3
rs1461347 0.882 0.120 11 37191871 intergenic variant T/C snv 4.5E-02 3
rs17138435 0.882 0.120 11 79481943 TF binding site variant A/C;G snv 1.6E-02 3
rs17167034 0.882 0.120 7 88488811 intron variant A/G snv 1.4E-02 3