Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 29
rs2227306
CXCL8
0.677 0.680 4 73741338 intron variant C/T snv 0.31 21
rs5029939
TNFAIP3
0.701 0.440 6 137874586 intron variant C/G snv 0.13 19
rs2227307
CXCL8
0.851 0.240 4 73740952 intron variant T/G snv 0.45 6
rs2076295
DSP
0.882 0.080 6 7562999 intron variant T/G snv 0.46 5
rs12602273
TP53
0.851 0.080 17 7679695 intron variant C/G snv 0.15 4
rs17690703
MAPT-AS1
0.882 0.160 17 45847931 intron variant C/T snv 0.18 4
rs5743890
TOLLIP
0.925 0.040 11 1304599 intron variant T/C snv 9.7E-02 4
rs628977
ADAM33
0.851 0.160 20 3669074 intron variant T/C snv 0.65 4
rs2305619
VEPH1 ; PTX3
0.882 0.240 3 157437072 intron variant A/G snv 0.55 0.50 3
rs733590
CDKN1A ; DINOL
0.882 0.120 6 36677426 intron variant T/C snv 0.41 3
rs2744371
DSP
0.925 0.080 6 7553941 intron variant A/C;G snv 2
rs111521887
TOLLIP
1.000 0.040 11 1291476 intron variant C/G snv 0.12 1
rs28673968
LOC105377329
1.000 0.040 4 89655739 intron variant T/C snv 0.37 1
rs5743894
LOC105376512 ; TOLLIP
1.000 0.040 11 1303542 intron variant T/A;C snv 1
rs8182352 0.827 0.160 17 5651667 intergenic variant T/C snv 0.44 5
rs1881984 1.000 0.040 3 169746671 intergenic variant A/G snv 0.30 1
rs113993959
CFTR
0.677 0.280 7 117587778 stop gained G/A;T snv 8.0E-06; 3.4E-04 25
rs74597325
CFTR
0.708 0.320 7 117587811 stop gained C/G;T snv 6.8E-05 18
rs397728201
SFTPA1
0.925 0.160 10 79614033 stop gained C/A;T snv 3.6E-05; 4.0E-06 4
rs398123017
RTEL1 ; RTEL1-TNFRSF6B
0.851 0.160 20 63693211 stop gained C/A;G;T snv 4.0E-06; 3.2E-05 4
rs1554043139
TERT
0.925 0.040 5 1294810 stop gained C/G;T snv 2
rs776525427
RTEL1-TNFRSF6B ; TNFRSF6B ; RTEL1
1.000 0.040 20 63695387 stop gained C/G;T snv 1.0E-05 7.0E-06 1
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226