Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6074022 0.851 0.240 20 46111557 TF binding site variant C/G;T snv 5
rs10876994 0.925 0.120 12 57670954 upstream gene variant A/C;T snv 2
rs28383224 0.925 0.160 6 32615876 regulatory region variant A/G snv 0.55 2
rs73366469 0.925 0.160 7 74619286 regulatory region variant T/C snv 0.12 2
rs2075575
AQP4-AS1 ; AQP4
0.851 0.200 18 26866562 intron variant G/A snv 0.31 5
rs150587304
AQP4-AS1 ; AQP4
1.000 0.120 18 26862573 stop gained C/A;G snv 3.2E-05; 2.9E-04 1
rs548234
ATG5
0.763 0.360 6 106120159 intron variant C/T snv 0.76 11
rs6937876
ATG5
0.925 0.200 6 106132754 intron variant G/A snv 0.70 2
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs4810485
CD40
0.732 0.480 20 46119308 intron variant T/A;G snv 16
rs3765459
CD40
0.807 0.280 20 46128768 intron variant G/A;C snv 0.22 7
rs1016140
CD58
1.000 0.120 1 116533925 non coding transcript exon variant G/T snv 0.15 1
rs56302466
CD58
1.000 0.120 1 116541336 intron variant T/C snv 0.16 1
rs12288280
CD6
1.000 0.120 11 60988884 intron variant G/A;T snv 1
rs773144793
CH25H
1.000 0.120 10 89207242 missense variant C/G snv 3.7E-05 7.0E-06 1
rs3808607
CYP7A1
0.716 0.400 8 58500365 upstream gene variant G/T snv 0.55 16
rs3761959
FCRL3
0.827 0.320 1 157699488 intron variant C/A;G;T snv 7
rs945635
FCRL3
0.882 0.200 1 157700500 5 prime UTR variant C/A;G snv 5.6E-05; 0.45 4
rs2282284
FCRL3
0.925 0.120 1 157678753 missense variant T/C snv 5.4E-02 5.4E-02 2
rs1411751
GPC5
0.925 0.120 13 92245255 intron variant G/A snv 0.16 2
rs3135388
HLA-DRA
0.807 0.240 6 32445274 downstream gene variant A/G snv 0.90 7
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs6897932
IL7R
0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 25