Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2738774 0.724 0.240 20 63637985 downstream gene variant G/A;C snv 14
rs2807264 0.724 0.240 X 136583619 downstream gene variant C/A snv 14
rs30187
ERAP1
0.732 0.360 5 96788627 missense variant T/A;C snv 0.62 14
rs4869313
ERAP2 ; ERAP1
0.724 0.240 5 96888176 intron variant T/A;G snv 14
rs55705316 0.724 0.240 1 206760172 regulatory region variant T/A;G snv 14
rs7660520 0.724 0.240 4 182824168 upstream gene variant G/A;C snv 14
rs7831697 0.724 0.240 8 137124061 regulatory region variant T/A;C;G snv 14
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 13
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 12
rs1893592
UBASH3A
0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 12
rs7530511
IL23R ; C1orf141
0.742 0.400 1 67219704 missense variant T/A;C snv 0.88 12
rs10036748
TNIP1
0.752 0.360 5 151078585 intron variant C/A;T snv 11
rs10516487
BANK1
0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 11
rs10748781 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 11
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 10
rs2294020
CCDC22
0.763 0.280 X 49246763 missense variant A/G;T snv 10
rs280519
TYK2
0.752 0.320 19 10362257 splice region variant A/C;G snv 0.50 10
rs3021097
IL10 ; IL19
0.752 0.440 1 206773289 5 prime UTR variant A/G snv 10
rs4845604
RORC
0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs549858786
IL1B
0.790 0.320 2 112836807 5 prime UTR variant T/A snv 10
rs3789604
RSBN1 ; AP4B1-AS1
0.776 0.360 1 113812320 synonymous variant T/A;C;G snv 8.5E-06; 1.3E-05; 0.17 9
rs11230563
LOC105369326 ; CD6
0.790 0.360 11 61008737 missense variant C/G;T snv 4.2E-06; 0.31 8
rs11676348 0.790 0.160 2 218145423 regulatory region variant C/G;T snv 8
rs2812378
CCL21
0.790 0.200 9 34710263 intron variant G/A;C snv 8