Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs3025058
MMP3
0.658 0.600 11 102845217 upstream gene variant -/C;G ins 2.8E-04 26
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 18
rs1815739
ACTN3
0.763 0.240 11 66560624 stop gained C/T snv 0.37 17
rs6570507
ADGRG6
0.827 0.240 6 142358435 intron variant G/A snv 0.47 13
rs5742612
LOC105369944 ; IGF1
0.752 0.440 12 102481086 intron variant A/G snv 5.6E-02 11
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
rs708567
IL17RC
0.807 0.200 3 9918386 missense variant C/T snv 0.46 0.51 6
rs4753426
MTNR1B
0.827 0.280 11 92968430 upstream gene variant T/C snv 0.49 6
rs6137473 0.827 0.280 20 21904055 intergenic variant G/A snv 0.61 5
rs12885713
CALM1
0.827 0.200 14 90397013 intron variant C/A;G;T snv 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