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
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs1799750
WTAPP1 ; MMP1
0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs2234767
FAS ; ACTA2
0.649 0.280 10 88989499 intron variant G/A;T snv 0.15 30
rs2227306
CXCL8
0.677 0.680 4 73741338 intron variant C/T snv 0.31 21
rs182052
ADIPOQ
0.701 0.440 3 186842993 intron variant G/A snv 0.38 19
rs2232365
FOXP3
0.716 0.480 X 49259429 intron variant T/C snv 16
rs3117582
BAG6 ; APOM
0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 14
rs1800012
COL1A1
0.763 0.320 17 50200388 intron variant C/A snv 0.14 13
rs1143633
IL1B
0.752 0.280 2 112832890 intron variant C/G;T snv 11
rs12149832
FTO
0.851 0.120 16 53808996 intron variant G/A snv 0.31 8
rs5030772
FASLG
0.790 0.320 1 172664210 intron variant A/G snv 9.9E-02 7
rs650108
MMP3
0.827 0.160 11 102838056 intron variant G/A snv 0.31 6
rs8044769
FTO
0.851 0.200 16 53805223 intron variant T/A;C;G snv 6
rs1034528
MTOR ; ANGPTL7
0.882 0.120 1 11189075 intron variant G/C snv 0.30 5
rs12885713
CALM1
0.827 0.200 14 90397013 intron variant C/A;G;T snv 5
rs7135617
ORAI1
0.827 0.240 12 121631099 intron variant T/C;G snv 5
rs12982744
DOT1L
0.925 0.040 19 2177194 intron variant C/A;G;T snv 4
rs10948172
SUPT3H ; LOC101929770
0.882 0.040 6 44809954 intron variant A/G snv 0.27 3
rs10974438
GLIS3
0.925 0.120 9 4291928 intron variant A/C snv 0.29 3
rs12901071
SMAD3
0.882 0.160 15 67078051 intron variant A/G snv 0.25 3
rs12901499
SMAD3
0.882 0.040 15 67078107 intron variant G/A snv 0.45 3