Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1128503
ABCB1
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
rs57095329
MIR3142HG
0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 25
rs2070959
UGT1A8 ; UGT1A7 ; UGT1A9 ; UGT1A10 ; UGT1A6
0.742 0.320 2 233693545 missense variant A/G snv 0.31 0.30 16
rs1064797102
OTUD6B-AS1 ; OTUD6B
0.827 0.120 8 91071136 splice acceptor variant A/G snv 15
rs3789243
ABCB1
0.776 0.120 7 87591570 intron variant A/G snv 0.50 14
rs4906902
GABRB3
0.724 0.200 15 26774621 intron variant A/G snv 0.15 14
rs1064797103
OTUD6B
0.827 0.280 8 91078597 missense variant A/G snv 9
rs10818488
C5-OT1
0.776 0.360 9 120942809 regulatory region variant A/G snv 0.51 8
rs587780455
SCN8A
0.827 0.160 12 51807116 missense variant A/G snv 7
rs587776954
RNU7-1 ; C12orf57
0.827 0.320 12 6944122 start lost A/G snv 3.2E-05 2.1E-05 6
rs1057518801
SCN3A
0.851 0.080 2 165130238 missense variant A/G snv 5
rs145999922
SLC19A3
0.882 0.040 2 227699378 missense variant A/G snv 4.4E-05 4.2E-05 5
rs443198
NOTCH4
0.851 0.200 6 32222629 synonymous variant A/G snv 0.38 0.39 4
rs118192249
KCNQ3
0.882 0.080 8 132175461 missense variant A/G snv 4.0E-06 3
rs730882226
INO80
0.925 0.120 15 41071953 missense variant A/G snv 1.6E-05 4.2E-05 3
rs12059546
CHRM3
0.925 0.040 1 239806797 intron variant A/G snv 0.30 2
rs121918363
SRPX2
0.925 0.200 X 100667292 missense variant A/G snv 5.7E-04 4.1E-04 2
rs13287547
C9orf92
1.000 0.040 9 16286892 intron variant A/G snv 0.32 2
rs199472904
KCNH2
0.925 0.160 7 150952595 missense variant A/G snv 2
rs2292096
CAMSAP2
0.925 0.040 1 200857641 3 prime UTR variant A/G snv 0.14 2
rs2304016
SCN2A
0.925 0.040 2 165311993 intron variant A/G snv 1.2E-02 4.8E-03 2
rs28898617
UGT1A8 ; UGT1A10 ; UGT1A3 ; UGT1A7 ; UGT1A4 ; UGT1A9 ; UGT1A5 ; UGT1A6
1.000 0.040 2 233729143 missense variant A/G snv 3.5E-03 1.1E-03 2
rs3773364
SYN2
0.925 0.040 3 12148468 intron variant A/G snv 0.15 2