Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 7
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 6
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 6
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 6
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs763361
CD226
0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 4
rs12708716
CLEC16A
0.807 0.320 16 11086016 intron variant A/G snv 0.37 4
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46 4
rs4750316
LINC02649 ; LINC02656
0.882 0.160 10 6351298 non coding transcript exon variant C/G;T snv 4
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 4
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 3
rs1980422 0.776 0.320 2 203745673 intergenic variant C/A;T snv 3
rs3807306
IRF5
0.776 0.320 7 128940626 intron variant G/A;T snv 3
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 2
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 2
rs1127354
ITPA
0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 2
rs11466018
MEFV
0.827 0.200 16 3254739 missense variant A/G snv 6.6E-03 2.2E-03 2
rs10931481
STAT4
0.827 0.240 2 191090126 intron variant G/A snv 0.66 2
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 2
rs2395148
TSBP1 ; TSBP1-AS1
0.882 0.200 6 32353777 intron variant G/T snv 4.6E-02 2
rs11817689 1.000 0.120 10 63164457 downstream gene variant T/C snv 0.13 1