Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs2569190
CD14 ; TMCO6
0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs1258159645
NQO1
0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs1800925
IL13 ; TH2LCRR
0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs1800624
PBX2 ; AGER
0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs4950928
CHI3L1
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs1982073
TGFB1
0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20 31
rs568408
IL12A ; IL12A-AS1
0.649 0.600 3 159995680 3 prime UTR variant G/A snv 0.16 29
rs137854539
GNAS
0.716 0.520 20 58903703 missense variant C/T snv 28
rs1294950721
JAG1
0.807 0.360 20 10645355 splice donor variant C/A;T snv 7.0E-06 27
rs2814778
CADM3-AS1 ; ACKR1
0.763 0.360 1 159204893 5 prime UTR variant T/C snv 0.25 24
rs4977756
CDKN2B-AS1
0.683 0.440 9 22068653 intron variant G/A snv 0.64 24
rs8034191
HYKK
0.695 0.440 15 78513681 intron variant T/C snv 0.27 24
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31 23
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48 22
rs1557055405
ABCD1
0.807 0.400 X 153743532 missense variant T/A snv 21
rs2227306
CXCL8
0.677 0.680 4 73741338 intron variant C/T snv 0.31 21
rs6010620
RTEL1 ; RTEL1-TNFRSF6B
0.701 0.360 20 63678486 intron variant A/C;G snv 21
rs8193036
IL17A
0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 21
rs2187668
LOC107986589 ; HLA-DQA2 ; HLA-DQA1
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 20
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 20
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs2069705
IFNG-AS1 ; IFNG
0.695 0.440 12 68161231 intron variant G/A;C snv 19