Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1340420
TNKS2
0.925 0.080 10 91857549 intron variant A/G snv 0.71 0.70 3
rs1770474
TNKS2
0.925 0.080 10 91833770 intron variant G/A;T snv 3
rs17568
TNFRSF4
0.752 0.320 1 1212042 synonymous variant C/T snv 0.37 0.31 12
rs2298211
TNFRSF4
1.000 0.040 1 1211863 intron variant A/C snv 8.1E-02 8.2E-02 1
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs7208422
TMC8
0.807 0.120 17 78134494 missense variant A/C;T snv 4.0E-06; 0.51 6
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs2736098
TERT
0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 29
rs771590775
TERT
1.000 0.040 5 1294350 missense variant C/A;G snv 1
rs1458974438
STK11
0.807 0.080 19 1206957 missense variant G/A snv 9
rs59912467
STK11
0.790 0.120 19 1223126 missense variant C/G;T snv 5.2E-03; 4.1E-06 7
rs1057520018
STK11
0.807 0.080 19 1223124 missense variant T/C snv 6
rs1057520039
STK11
0.882 0.200 19 1207169 stop gained C/G;T snv 4
rs2239612
ST6GAL1
1.000 0.040 3 187075454 intron variant G/A snv 0.17 2
rs754626
SRC
0.925 0.080 20 37388937 intron variant T/G snv 0.25 2
rs35063026
SPATA33
0.925 0.080 16 89669749 3 prime UTR variant C/T snv 4.7E-02 3
rs17761864
SMG6
1.000 0.040 17 2268343 intron variant C/A snv 0.28 2
rs4149056
SLCO1B1
0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 45
rs16891982
SLC45A2
0.776 0.200 5 33951588 missense variant C/A;G snv 0.65 13
rs35407
SLC45A2
0.807 0.080 5 33946466 3 prime UTR variant A/C;G snv 6
rs1050631
SLC39A6
0.882 0.080 18 36114157 synonymous variant G/A snv 0.33 0.30 4
rs10759637
SLC31A1 ; CDC26
1.000 0.040 9 113262744 3 prime UTR variant A/C snv 0.47 2