Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs10465885
LOC102723321 ; GJA5
0.882 0.080 1 147760632 intron variant T/A;C snv 4
rs1053004
STAT3
0.776 0.280 17 42314074 3 prime UTR variant G/A snv 0.48 11
rs1056744559
TLR4
1.000 0.080 9 117713974 stop gained C/G;T snv 4.0E-06; 2.8E-05 1
rs1061624
TNFRSF1B
0.776 0.320 1 12207208 3 prime UTR variant A/G snv 0.48 8
rs10853728 0.851 0.160 19 39254506 downstream gene variant C/A;G;T snv 5
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs11536889
TLR4
0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11 27
rs117648444
IFNL4
0.882 0.160 19 39247938 missense variant G/A snv 0.25 8.1E-02 3
rs11977021 0.827 0.240 7 106288069 upstream gene variant C/T snv 0.22 5
rs120074192
KCNQ1
0.763 0.120 11 2527959 missense variant A/G snv 10
rs12508721
IL21-AS1
0.742 0.360 4 122623509 intron variant C/T snv 0.24 11
rs1265163
POU5F1 ; TCF19
1.000 0.080 6 31166310 missense variant C/G;T snv 0.14; 7.2E-06 1
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs13419896
EPAS1
0.776 0.240 2 46329206 intron variant G/A snv 0.10 8
rs1419881
TCF19
0.851 0.280 6 31162816 3 prime UTR variant G/A snv 0.50 4
rs142346548
IFNL3
0.925 0.160 19 39244145 missense variant G/A snv 4.0E-06 2
rs171941
LOC105379048
1.000 0.080 5 79884303 intergenic variant G/A;T snv 1
rs17401966
KIF1B
0.790 0.280 1 10325413 intron variant A/G snv 0.24 7
rs17408553
HLA-C ; HLA-B
0.925 0.080 6 31271630 missense variant G/A;T snv 0.37 2
rs179009
TLR7
0.925 0.160 X 12885361 intron variant A/G;T snv 2
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1800470
TGFB1
0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1800472
TGFB1
0.752 0.360 19 41341955 missense variant G/A snv 2.6E-02 2.3E-02 11
rs1805011
IL4R
0.776 0.320 16 27362551 missense variant A/C;G;T snv 0.13; 1.2E-04; 3.6E-05 8