Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs35761398
CNR2
0.701 0.520 1 23875429 missense variant TT/CC mnv 19
rs5744174
TLR5
0.742 0.360 1 223111186 missense variant A/G snv 0.39 0.34 13
rs3811381
CR1
0.763 0.240 1 207616743 missense variant C/A;G snv 8.0E-06; 0.24 11
rs2274567
CR1
0.776 0.400 1 207580276 missense variant A/G snv 0.25 0.21 10
rs1061624
TNFRSF1B
0.776 0.320 1 12207208 3 prime UTR variant A/G snv 0.48 8
rs17401966
KIF1B
0.790 0.280 1 10325413 intron variant A/G snv 0.24 7
rs2070150
ATF6
0.827 0.280 1 161791486 missense variant G/C snv 0.14 9.2E-02 6
rs10465885
LOC102723321 ; GJA5
0.882 0.080 1 147760632 intron variant T/A;C snv 4
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs13419896
EPAS1
0.776 0.240 2 46329206 intron variant G/A snv 0.10 8
rs6715787
EPAS1
0.851 0.200 2 46349033 intron variant C/G;T snv 4
rs763809932
TTN ; TTN-AS1
1.000 0.080 2 178614110 missense variant G/A;T snv 2.4E-05 1.4E-05 1
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20 31
rs414171
MAPKAPK3 ; CISH
0.790 0.200 3 50612068 5 prime UTR variant A/G;T snv 9
rs199473565
SCN5A
0.882 0.120 3 38606743 missense variant C/T snv 4.0E-06 7.0E-06 3
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
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
rs907715
IL21
0.752 0.520 4 122613898 intron variant C/T snv 0.35 11
rs2853744
SPP1
0.882 0.200 4 87975096 non coding transcript exon variant G/T snv 0.14 4
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs2736098
TERT
0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48