Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs71559680 0.827 0.120 6 21430497 intergenic variant TAG/CAT mnv 6
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs3212227
IL12B
0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37 19
rs2395029
HCP5
0.790 0.320 6 31464003 non coding transcript exon variant T/G snv 2.7E-02 2.4E-02 12
rs11465804
IL23R
0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 10
rs1569414
FAM118A
0.807 0.160 22 45331684 intron variant T/G snv 0.44 6
rs34779708
CREM
0.827 0.120 10 35177257 intron variant T/G snv 0.33 6
rs3776414
DAP
0.827 0.120 5 10689450 intron variant T/G snv 0.48 6
rs4243971 0.827 0.120 20 32261714 intergenic variant T/G snv 0.64 6
rs111305875 0.827 0.120 6 167098098 intron variant T/G snv 3.0E-02 5
rs12987977
IL18R1
0.827 0.120 2 102358876 intron variant T/G snv 0.31 5
rs4085613 0.827 0.160 1 152577542 downstream gene variant T/G snv 0.59 5
rs6425143 0.827 0.120 1 172875212 intron variant T/G snv 0.34 5
rs130067
CCHCR1
0.851 0.200 6 31150734 missense variant T/G snv 0.23 0.21 4
rs3134792
HLA-B
0.851 0.280 6 31344549 intron variant T/G snv 8.8E-02 4
rs10789285 1.000 0.040 1 69322799 intergenic variant T/G snv 0.33 2
rs8016947 0.925 0.080 14 35363460 intron variant T/G snv 0.60 2
rs12972990
ICAM5
1.000 0.040 19 10295755 intron variant T/G snv 0.35 1
rs771797724
DCLRE1C
1.000 0.040 10 14908688 missense variant T/G snv 1.6E-05 7.0E-06 1
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83