Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5844572
MIF ; MIF-AS1
0.752 0.360 22 23893562 intron variant -/ATTC delins 11
rs1032129
TNFRSF11B
0.851 0.040 8 118939661 intron variant A/C snv 0.37 5
rs11073337
RASGRP1
0.851 0.040 15 38555562 intron variant A/C snv 0.27 5
rs1199047
CCDC88B
0.882 11 64350711 intron variant A/C snv 0.38 4
rs10892286
DDX6
11 118771376 intron variant A/C snv 0.17 2
rs17758761
ANKFN1
1.000 0.080 17 55977164 intron variant A/C snv 4.1E-02 2
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 12
rs104895271
TNFRSF1A
0.851 0.240 12 6334161 missense variant A/C;G snv 1.6E-04; 4.8E-05 6
rs1250552
ZMIZ1
0.882 0.200 10 79298270 intron variant A/C;G snv 5
rs13010713
LINC01934
0.882 0.200 2 181131318 intron variant A/C;G snv 5
rs9792269 0.882 0.200 8 128252343 intergenic variant A/C;G snv 5
rs1310182
AP4B1-AS1 ; PTPN22
0.882 0.360 1 113830881 intron variant A/C;G snv 0.56 4
rs1921445 0.882 3 106229671 intergenic variant A/C;G snv 4
rs2456973
LOC105369781 ; IKZF4 ; LOC105369780
0.925 0.040 12 56023144 intron variant A/C;G snv 4
rs6848139 1.000 0.040 4 122473886 intergenic variant A/C;G snv 3
rs4288027
KIAA1109
4 122262050 intron variant A/C;G snv 0.13 2
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs10735810
VDR
0.662 0.640 12 47879112 start lost A/C;G;T snv 26
rs11145763
CARD9
0.724 0.240 9 136369144 intron variant A/C;G;T snv 14
rs396991
FCGR3A
0.742 0.480 1 161544752 missense variant A/C;G;T snv 0.33; 4.1E-06 14
rs391851 0.882 5 103342219 intergenic variant A/C;G;T snv 4
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 19
rs179008
TLR7
0.763 0.360 X 12885540 missense variant A/C;T snv 0.18 0.18 14
rs8061370
LOC105371082 ; RMI2
0.882 16 11364614 intron variant A/C;T snv 4