Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 9
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 9
rs185819
TNXB
0.851 0.200 6 32082290 missense variant T/A;C;G snv 8.2E-06; 0.58; 4.1E-06 8
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs2844511 0.807 0.200 6 31422007 intron variant A/G;T snv 7
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 7
rs3130618
CSNK2B ; GPANK1
0.827 0.360 6 31664357 missense variant C/A;T snv 0.15; 4.0E-06 6
rs527476195
PSORS1C1
0.925 0.120 6 31133165 intron variant G/A snv 6
rs6457617 0.763 0.480 6 32696074 intergenic variant C/A;T snv 6
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 5
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 5
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 5
rs2239804
HLA-DRA
0.851 0.240 6 32443746 intron variant T/A;C snv 0.51 5
rs2844529 0.925 0.120 6 31385816 upstream gene variant G/A;T snv 5
rs2844795
TRIM31 ; TRIM31-AS1
0.925 0.120 6 30106070 intron variant C/G;T snv 5
rs3129890 0.827 0.280 6 32446496 downstream gene variant T/A;C snv 5
rs3806156
BTNL2 ; TSBP1-AS1
0.827 0.280 6 32405921 intron variant G/A;T snv 5
rs615672
HLA-DRB1
0.851 0.240 6 32606394 intergenic variant G/A;C snv 5
rs6903608
HLA-DRB9
0.742 0.400 6 32460508 intron variant C/G;T snv 5
rs9268645
HLA-DRA
0.827 0.360 6 32440750 intron variant C/G;T snv 5
rs11066188
HECTD4
0.851 0.320 12 112172910 intron variant G/A;C snv 0.30; 4.1E-06 4
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 4
rs204990
GPSM3
0.851 0.280 6 32193653 intron variant C/A;T snv 4
rs2201841
C1orf141 ; IL23R
0.716 0.440 1 67228519 intron variant A/G;T snv 4
rs3134603
PPT2-EGFL8 ; PPT2
0.851 0.360 6 32158225 non coding transcript exon variant A/C;G;T snv 4