Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 23
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46 15
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 10
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 9
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 8
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 7
rs10488631
TNPO3
0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 7
rs7579944 0.882 0.200 2 30222160 intergenic variant T/C;G snv 5
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 4
rs3130544 0.807 0.360 6 31090563 intergenic variant C/A snv 7.4E-02 4
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 4
rs802734 0.827 0.280 6 127957653 intergenic variant A/G;T snv 4
rs6840978
IL21-AS1
0.776 0.160 4 122633552 intron variant C/T snv 0.16 4
rs11203203
UBASH3A
0.807 0.240 21 42416077 intron variant G/A snv 0.28 4
rs10892279 1.000 0.120 11 118741072 intron variant G/A;T snv 0.25 3
rs6933404 0.925 0.280 6 137638098 intergenic variant T/C snv 0.16 3
rs864537
CD247
0.925 0.200 1 167442147 intron variant A/G snv 0.29 3
rs4810485
CD40
0.732 0.480 20 46119308 intron variant T/A;G snv 3
rs212388
LOC112267968 ; LOC105378083
0.827 0.240 6 159069404 intron variant C/G;T snv 3
rs13003464
PUS10
0.827 0.200 2 60959694 intron variant A/G snv 0.50 3
rs2298428
YDJC
0.807 0.240 22 21628603 missense variant C/T snv 0.27 0.18 3
rs1020388 5 56264200 upstream gene variant T/G snv 0.34 2
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 2