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
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31 23
rs352139
TLR9
0.732 0.320 3 52224356 intron variant T/C snv 0.51 0.54 18
rs3761549
FOXP3
0.724 0.480 X 49260888 intron variant G/A snv 9.6E-02 18
rs2232365
FOXP3
0.716 0.480 X 49259429 intron variant T/C snv 16
rs2069727
IFNG ; IFNG-AS1
0.763 0.320 12 68154443 intron variant T/A;C snv 9
rs4693608
HPSE
0.827 0.200 4 83320204 intron variant G/A;C snv 6
rs4845618
IL6R
0.851 0.160 1 154427539 intron variant G/T snv 0.53 5
rs9277378
HLA-DPB1 ; HLA-DPA1
0.827 0.320 6 33082502 intron variant A/G snv 0.40 5
rs4364254
HPSE
0.882 0.080 4 83302560 intron variant C/T snv 0.63 3
rs7588571
REG3A
0.882 0.040 2 79161461 intron variant G/A snv 0.49 3
rs3092936
CD40LG
1.000 0.040 X 136654046 intron variant T/C snv 8.9E-02 2
rs4833079
KLF3-AS1
1.000 0.040 4 38653060 intron variant T/C snv 0.30 2
rs6531656
KLF3
1.000 0.040 4 38682580 intron variant C/T snv 0.87 2
rs2310241
IL1RL2
1.000 0.040 2 102225489 intron variant A/C snv 0.44 1
rs337629
KLF3-AS1
1.000 0.040 4 38633737 intron variant A/G;T snv 1
rs10737416
LOC105373109
1.000 0.040 1 224887055 intergenic variant C/A;T snv 1
rs4837656 1.000 0.040 9 119671775 intergenic variant T/C snv 0.27 1
rs17582214 1.000 0.040 9 119676531 regulatory region variant A/G;T snv 1
rs16910526
CLEC7A ; LOC105369655
0.742 0.280 12 10118488 stop gained A/C;G snv 6.2E-02 12
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs6897932
IL7R
0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 25
rs1129055
CD86
0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25 15