Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28359178
CYTB ; ND5 ; ND6
0.882 0.280 MT 13708 missense variant G/A snv 3
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs2232365
FOXP3
0.716 0.480 X 49259429 intron variant T/C snv 16
rs3027898
IRAK1
0.752 0.360 X 154010439 downstream gene variant C/A snv 11
rs2294020
CCDC22
0.763 0.280 X 49246763 missense variant A/G;T snv 10
rs3761547
FOXP3
0.882 0.200 X 49262004 intron variant T/C snv 9.6E-02 3
rs391745 0.925 0.080 X 97839482 intergenic variant C/G;T snv 3
rs1044165
VSIG4
1.000 0.080 X 66021884 3 prime UTR variant G/A snv 9.0E-02 1
rs132630295
RAB9B ; PLP1
1.000 0.080 X 103786682 missense variant C/T snv 1
rs4271113 1.000 0.080 X 34874386 regulatory region variant G/A snv 0.14 1
rs5945430
PLXNA3
1.000 0.080 X 154465991 missense variant G/C snv 1
rs6622139 1.000 0.080 X 107053120 intergenic variant T/C snv 0.36 1
rs72619425 1.000 0.080 X 37753178 intron variant C/T snv 0.21 1
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs755622
MIF-AS1 ; MIF
0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs1232898090
PPARA
0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 38
rs1800206
PPARA
0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs1445081098
COMT ; MIR4761
0.724 0.480 22 19963746 missense variant G/C snv 4.0E-06 17
rs749437638
ARVCF ; COMT
0.752 0.240 22 19968597 missense variant C/T snv 2.4E-05 1.4E-05 14
rs140522
ODF3B
0.851 0.160 22 50532837 upstream gene variant T/A;C snv 11
rs5844572
MIF ; MIF-AS1
0.752 0.360 22 23893562 intron variant -/ATTC delins 11
rs6971
TSPO
0.742 0.200 22 43162920 missense variant A/G snv 0.76 0.75 11
rs229541
C1QTNF6
0.807 0.200 22 37195278 intron variant G/A snv 0.49 8
rs743777
IL2RB
0.827 0.200 22 37155567 intron variant A/G snv 0.36 7