Disease: Autoimmune Diseases
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2228044
IL6ST
0.882 0.240 5 55968325 missense variant C/G snv 0.13 0.21 5
rs3731865
SLC11A1
0.882 0.160 2 218385280 non coding transcript exon variant G/A;C;T snv 0.23; 1.4E-04 5
rs4750316
LINC02649 ; LINC02656
0.882 0.160 10 6351298 non coding transcript exon variant C/G;T snv 5
rs745826707
RBM45
0.851 0.200 2 178112712 missense variant G/A;T snv 8.0E-06; 4.0E-06 5
rs7579944 0.882 0.200 2 30222160 intergenic variant T/C;G snv 5
rs104895271
TNFRSF1A
0.851 0.240 12 6334161 missense variant A/C;G snv 1.6E-04; 4.8E-05 6
rs1059703
IRAK1
0.851 0.280 X 154013378 missense variant G/A snv 0.67 6
rs11264799
FCRL3
0.851 0.240 1 157700967 upstream gene variant C/T snv 0.28 6
rs1059702
IRAK1
0.807 0.280 X 154018741 missense variant A/G snv 0.72 7
rs17266594
BANK1
0.807 0.280 4 101829765 intron variant T/C snv 0.25 0.27 7
rs3093023
LOC105378122 ; CCR6
0.851 0.160 6 167120802 intron variant G/A snv 0.34 7
rs3761959
FCRL3
0.827 0.320 1 157699488 intron variant C/A;G;T snv 7
rs71508903
ARID5B
0.807 0.160 10 62020112 intron variant C/T snv 0.15 7
rs743777
IL2RB
0.827 0.200 22 37155567 intron variant A/G snv 0.36 7
rs13119723
KIAA1109
0.807 0.280 4 122297158 intron variant A/G snv 0.10 8
rs3761847
TRAF1
0.827 0.200 9 120927961 intron variant G/A snv 0.52 8
rs11203203
UBASH3A
0.807 0.240 21 42416077 intron variant G/A snv 0.28 9
rs1678542
KIF5A
0.790 0.320 12 57574932 intron variant C/G snv 0.42 9
rs1738074
LOC105378083 ; LOC107986664 ; TAGAP
0.790 0.320 6 159044945 5 prime UTR variant T/C snv 0.49 9
rs1980422 0.776 0.320 2 203745673 intergenic variant C/A;T snv 9
rs35018800
TYK2
0.790 0.160 19 10354167 missense variant G/A snv 4.6E-03 4.9E-03 9
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
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs3811047
IL37
0.807 0.400 2 112913833 missense variant A/G snv 0.71 0.60 10
rs951005 0.807 0.200 9 34743684 intron variant G/A snv 0.78 10