Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 23
rs2243268
IL4
0.882 0.040 5 132678271 intron variant A/C snv 0.23 3
rs4262994 1.000 0.040 17 37591398 intron variant A/C snv 0.17 2
rs1449626 1.000 0.040 11 47269208 5 prime UTR variant A/C snv 0.26 1
rs4733781 1.000 0.040 8 130284521 intron variant A/C snv 0.29 1
rs2069837 0.724 0.520 7 22728408 intron variant A/C;G snv 18
rs3751143 0.742 0.480 12 121184501 missense variant A/C;G snv 0.19; 4.0E-06 12
rs9298814 0.790 0.160 9 21227623 missense variant A/C;G snv 0.12; 8.8E-06 7
rs2723176 0.851 0.200 2 112914932 intron variant A/C;G snv 4
rs755017 0.925 0.080 20 63790269 synonymous variant A/C;G snv 0.17 2
rs12654043 1.000 0.040 5 150846533 5 prime UTR variant A/C;G snv 1
rs3948464 1.000 0.040 2 230185999 missense variant A/C;G snv 8.0E-06; 0.89 1
rs755508039 1.000 0.040 6 159907236 missense variant A/C;G snv 1
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs10735810
VDR
0.662 0.640 12 47879112 start lost A/C;G;T snv 26
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs9268494 0.882 0.200 6 32407575 non coding transcript exon variant A/C;T snv 0.32 3
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs1128503 0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs2569190 0.620 0.560 5 140633331 intron variant A/G snv 0.57 39