Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs179008
TLR7
0.763 0.360 X 12885540 missense variant A/C;T snv 0.18 0.18 14
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs2427216
CDH4
1.000 0.040 20 61639158 intron variant C/A;T snv 1
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 25
rs206530
LOC105371989
0.925 0.040 18 10394467 downstream gene variant T/C snv 0.70 2
rs2847260 1.000 0.040 18 12775592 non coding transcript exon variant C/T snv 0.82 1
rs6502976
XAF1
1.000 0.040 17 6764511 intron variant C/G snv 0.49 1
rs9905945 1.000 0.040 17 63461695 regulatory region variant C/G;T snv 1
rs2066845
NOD2
0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 46
rs3917200
TGFB3 ; IFT43
0.882 0.080 14 75963525 intron variant A/G snv 9.2E-02 0.14 3
rs10162249
ATP8A2
1.000 0.040 13 25849519 intron variant T/C snv 0.14 1
rs10467674
ATP8A2
1.000 0.040 13 25854100 intron variant T/A snv 0.14 1
rs112198380
ATP8A2
1.000 0.040 13 25855238 intron variant A/G snv 0.14 1
rs12020004
ATP8A2
1.000 0.040 13 25851513 intron variant G/A snv 0.13 1
rs12858139
FLT1
1.000 0.040 13 28483931 intron variant A/C snv 0.44 1
rs2296283
FLT1
1.000 0.040 13 28389565 3 prime UTR variant G/A snv 0.42 1
rs61949368
ATP8A2
1.000 0.040 13 25854979 intron variant G/A snv 0.13 1
rs9319247
ATP8A2
1.000 0.040 13 25848959 intron variant T/C;G snv 1
rs9319248
ATP8A2
1.000 0.040 13 25849030 intron variant C/A snv 0.13 1
rs9319249
ATP8A2
1.000 0.040 13 25854051 intron variant T/C snv 0.14 1
rs9319250
ATP8A2
1.000 0.040 13 25854469 intron variant T/C;G snv 1
rs9507586
ATP8A2
1.000 0.040 13 25852156 intron variant A/T snv 0.14 1
rs9507587
ATP8A2
1.000 0.040 13 25852362 intron variant G/A snv 0.14 1
rs9507588
ATP8A2
1.000 0.040 13 25852698 intron variant C/T snv 0.14 1
rs9507589
ATP8A2
1.000 0.040 13 25852835 intron variant T/C snv 0.13 1