Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 12
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 7
rs6457617 0.763 0.480 6 32696074 intergenic variant C/A;T snv 6
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 6
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 5
rs540385376
PSORS1C1 ; CDSN
0.925 0.120 6 31117605 non coding transcript exon variant C/A snv 5
rs6903608
HLA-DRB9
0.742 0.400 6 32460508 intron variant C/G;T snv 5
rs2201841
C1orf141 ; IL23R
0.716 0.440 1 67228519 intron variant A/G;T snv 4
rs763361
CD226
0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 4
rs4947296 0.851 0.440 6 31090401 intergenic variant T/A;C snv 3
rs1024161 0.925 0.160 2 203857029 intergenic variant T/A;C snv 2
rs229527
C1QTNF6
0.925 0.160 22 37185445 missense variant C/A;G snv 0.43 2
rs3118470
IL2RA
0.752 0.360 10 6059750 intron variant T/A;C snv 2
rs534526282
PSORS1C1
1.000 0.120 6 31123496 intron variant G/C snv 2
rs6909253 0.925 0.200 6 30087866 intergenic variant G/A;T snv 2
rs10197319 1.000 0.120 2 203898321 regulatory region variant G/A;T snv 1
rs11571302 0.925 0.200 2 203878211 downstream gene variant G/A;T snv 1
rs12050151
CEP128
1.000 0.120 14 80902473 intron variant T/C;G snv 1
rs1610591 1.000 0.120 6 29710058 upstream gene variant A/G;T snv 1
rs2075580
DDX39B ; ATP6V1G2-DDX39B ; SNORD117
1.000 0.120 6 31536198 intron variant G/A;C snv 1
rs2254071 1.000 0.120 6 29838285 intergenic variant T/C;G snv 1
rs2273017
TSBP1 ; TSBP1-AS1
1.000 0.120 6 32369853 intron variant G/A;C snv 0.59 1
rs2516512
MICB-DT
1.000 0.120 6 31480786 non coding transcript exon variant C/A;T snv 1
rs2900180
C5-OT1
0.827 0.280 9 120944104 regulatory region variant T/A;C snv 1
rs3132613
ABCF1 ; ABCF1-DT
1.000 0.120 6 30569829 upstream gene variant C/A;G snv 1