Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs3748067
IL17A
0.672 0.320 6 52190541 3 prime UTR variant C/T snv 6.2E-02 21
rs8193036
IL17A
0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 21
rs148704956
IL17A
0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06 19
rs3819024
IL17A
0.701 0.560 6 52185988 upstream gene variant A/G snv 0.34 17
rs4711998
IL17A
0.708 0.360 6 52185555 upstream gene variant A/G snv 0.64 16
rs8193037
IL17A
0.752 0.320 6 52186311 upstream gene variant G/A;T snv 12
rs3819025
IL17A
0.752 0.480 6 52186476 intron variant G/A snv 0.13 8.5E-02 11
rs7747909
IL17A
0.790 0.320 6 52189451 3 prime UTR variant G/A snv 0.18 7
rs1974226
IL17A
0.827 0.240 6 52190537 3 prime UTR variant C/T snv 0.15 6
rs10484879
IL17A
0.827 0.160 6 52187159 intron variant G/A;T snv 5
rs3804513
IL17A
0.851 0.080 6 52188399 intron variant A/T snv 2.4E-02 4
rs3748068
IL17A
0.925 0.080 6 52190537 3 prime UTR variant C/T snv 2
rs8193038
IL17A
0.925 0.080 6 52186584 intron variant A/G snv 2.2E-02 2
rs1327295035
IL17A
1.000 0.200 6 52187730 missense variant A/G snv 1
rs1360218267
IL17A
1.000 0.080 6 52187734 synonymous variant C/T snv 4.0E-06 1
rs17878530
IL17A
1.000 0.080 6 52189247 synonymous variant C/A;T snv 4.0E-06; 8.4E-05 1
rs17880588
IL17A
1.000 0.080 6 52189226 synonymous variant G/A snv 4.5E-03 1.8E-02 1
rs201890924
IL17A
1.000 0.200 6 52187736 missense variant G/A snv 5.2E-05 2.8E-05 1