Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs78545931 0.925 0.080 2 102265892 intergenic variant A/G snv 0.16 2
rs892225
SBNO2
0.925 0.080 19 1152657 intron variant A/G snv 0.39 2
rs9893132 0.925 0.080 17 40598769 upstream gene variant A/G snv 0.59 2
rs4679858
IQCJ-SCHIP1 ; SCHIP1
1.000 0.080 3 159428036 intron variant A/G snv 0.16 1
rs7209742 1.000 0.080 17 39952455 upstream gene variant A/G snv 0.69 1
rs7218742
GSDMA
1.000 0.080 17 39958108 intron variant A/G snv 0.70 1
rs920672
NAV2
1.000 0.080 11 20028597 intron variant A/G snv 2.3E-02 1
rs4794820
LRRC3C
0.790 0.160 17 39933091 intron variant A/G;T snv 9
rs4065275
ORMDL3
0.807 0.160 17 39924612 intron variant A/G;T snv 0.56 6
rs5491
ICAM1
0.827 0.160 19 10274864 missense variant A/G;T snv 4.0E-06; 2.8E-02 6
rs992969 0.882 0.080 9 6209697 intergenic variant A/G;T snv 4
rs10158467 0.925 0.080 1 173162354 regulatory region variant A/G;T snv 2
rs5953283
PPP1R3F
0.925 0.080 X 49283326 intron variant A/G;T snv 2
rs7626218
TBL1XR1
0.925 0.080 3 177134250 intron variant A/T snv 0.41 3
rs56308324
TBX21
0.925 0.080 17 47741840 intron variant A/T snv 9.3E-02 2
rs76830467
NOS1
1.000 0.080 12 117321510 intron variant A/T snv 3.4E-02 2
rs201541519 1.000 0.080 14 105694756 intergenic variant AAGA/- delins 1.2E-02 2
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs5743618
TLR1
0.677 0.360 4 38797027 missense variant C/A snv 0.53 0.51 25
rs11236797 0.790 0.200 11 76588605 upstream gene variant C/A snv 0.39 8
rs2069763
IL2
0.807 0.320 4 122456327 synonymous variant C/A snv 0.36 0.29 6
rs117710327 0.882 0.080 19 33235672 TF binding site variant C/A snv 5.0E-02 5
rs6594499 0.882 0.120 5 111134439 downstream gene variant C/A snv 0.56 4
rs117420762
SLC2A10
1.000 0.080 20 46719767 intron variant C/A snv 5.8E-03 2
rs2388639 0.925 0.080 16 54455881 regulatory region variant C/A snv 0.23 2