Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1394220
LOC105377891
1.000 0.080 6 90309585 intron variant A/C snv 0.34 1
rs990171 1.000 0.080 2 102470310 upstream gene variant A/C snv 0.78 1
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
rs1893592
UBASH3A
0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 2
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 12
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 8
rs13003464
PUS10
0.827 0.200 2 60959694 intron variant A/G snv 0.50 7
rs17810546
IL12A-AS1
0.827 0.440 3 159947262 intron variant A/G snv 8.2E-02 6
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 6
rs3748816
MMEL1
0.827 0.200 1 2595307 missense variant A/G snv 0.41 0.46 6
rs10903122 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 5
rs13119723
KIAA1109
0.807 0.280 4 122297158 intron variant A/G snv 0.10 5
rs13151961
KIAA1109
0.827 0.200 4 122194347 intron variant A/G snv 0.11 5
rs864537
CD247
0.925 0.200 1 167442147 intron variant A/G snv 0.29 4
rs9286879 0.851 0.200 1 172893094 intron variant A/G snv 0.32 4
rs9357152 0.827 0.240 6 32697183 regulatory region variant A/G snv 0.24 4
rs13132308
IL21-AS1
0.807 0.160 4 122629959 intron variant A/G snv 0.10 1
rs182429
LOC107986664 ; LOC105378083
1.000 0.080 6 159048542 intron variant A/G snv 0.49 1
rs6715106
STAT4
1.000 0.080 2 191048308 intron variant A/G snv 6.1E-02 1
rs79758729
ELMO1
1.000 0.080 7 37378851 intron variant A/G snv 7.9E-02 1
rs8081319
ACACA ; C17orf78
1.000 0.080 17 37374139 intron variant A/G snv 6.8E-02 1
rs936229
ULK3
1.000 0.080 15 74839978 intron variant A/G snv 0.67 1