Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17401966
KIF1B
0.790 0.280 1 10325413 intron variant A/G snv 0.24 7
rs61330082
NAMPT
0.732 0.320 7 106286419 upstream gene variant G/A snv 0.22 13
rs11977021 0.827 0.240 7 106288069 upstream gene variant C/T snv 0.22 5
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1056744559
TLR4
1.000 0.080 9 117713974 stop gained C/G;T snv 4.0E-06; 2.8E-05 1
rs11536889
TLR4
0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11 27
rs676925
CXCR5 ; BCL9L
1.000 0.080 11 118894979 3 prime UTR variant C/G snv 0.20 1
rs1061624
TNFRSF1B
0.776 0.320 1 12207208 3 prime UTR variant A/G snv 0.48 8
rs907715
IL21
0.752 0.520 4 122613898 intron variant C/T snv 0.35 11
rs2221903
IL21-AS1 ; IL21
0.752 0.360 4 122617757 intron variant C/T snv 0.77 12
rs12508721
IL21-AS1
0.742 0.360 4 122623509 intron variant C/T snv 0.24 11
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs2242652
TERT
0.724 0.400 5 1279913 intron variant G/A snv 0.18 16
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs179009
TLR7
0.925 0.160 X 12885361 intron variant A/G;T snv 2
rs2280714
TNPO3
0.752 0.440 7 128954671 3 prime UTR variant C/T snv 0.64 10
rs2736098
TERT
0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs10465885
LOC102723321 ; GJA5
0.882 0.080 1 147760632 intron variant T/A;C snv 4
rs2070150
ATF6
0.827 0.280 1 161791486 missense variant G/C snv 0.14 9.2E-02 6
rs763809932
TTN ; TTN-AS1
1.000 0.080 2 178614110 missense variant G/A;T snv 2.4E-05 1.4E-05 1
rs3775291
TLR3
0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs3775290
TLR3
0.742 0.280 4 186083063 missense variant C/A;T snv 0.30 15
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs2274567
CR1
0.776 0.400 1 207580276 missense variant A/G snv 0.25 0.21 10
rs3811381
CR1
0.763 0.240 1 207616743 missense variant C/A;G snv 8.0E-06; 0.24 11