Source: GWASDB ×
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 24
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
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 8
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 7
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 7
rs13003464
PUS10
0.827 0.200 2 60959694 intron variant A/G snv 0.50 7
rs10488631
TNPO3
0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 7
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 6
rs3130544 0.807 0.360 6 31090563 intergenic variant C/A snv 7.4E-02 6
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 6
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 6
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 6
rs17810546
IL12A-AS1
0.827 0.440 3 159947262 intron variant A/G snv 8.2E-02 6
rs9264942
LOC112267902 ; HLA-B
0.763 0.400 6 31306603 intron variant T/C snv 0.34 6
rs3748816
MMEL1
0.827 0.200 1 2595307 missense variant A/G snv 0.41 0.46 6
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 6
rs10903122 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 5
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 5
rs802734 0.827 0.280 6 127957653 intergenic variant A/G;T snv 5
rs9792269 0.882 0.200 8 128252343 intergenic variant A/C;G snv 5
rs11712165
ARHGAP31
0.882 0.200 3 119399949 intron variant T/G snv 0.30 5
rs10806425
BACH2
0.851 0.280 6 90216893 intron variant C/A snv 0.33 5
rs13098911
CCR3
0.882 0.200 3 46193709 intron variant C/G;T snv 5