Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs10796045 1.000 0.080 10 6360779 intergenic variant G/T snv 0.79 1
rs947474
LINC02649 ; LINC02656
0.827 0.440 10 6348488 intron variant G/A snv 0.79 3
rs2816316
LOC105371664
0.882 0.200 1 192567683 intron variant C/A snv 0.79 5
rs990171 1.000 0.080 2 102470310 upstream gene variant A/C snv 0.78 1
rs6498114
CIITA ; LOC105371080
1.000 0.080 16 10870261 intron variant G/T snv 0.78 1
rs13015714
IL18R1
0.882 0.200 2 102355405 intron variant G/T snv 0.77 2
rs2249937
LOC112267968
1.000 0.080 6 159094277 non coding transcript exon variant T/G snv 0.76 3
rs169858
LOC105378083 ; LOC112267968
1.000 0.080 6 159063744 intron variant T/C snv 0.76 1
rs6441961
UQCRC2P1
1.000 0.080 3 46310893 non coding transcript exon variant T/C snv 0.74 1
rs11711054 1.000 0.080 3 46304120 intergenic variant G/A snv 0.73 1
rs2474619
BACH2
0.882 0.360 6 90170316 intron variant C/A snv 0.72 1
rs2097282 1.000 0.080 3 46336534 intergenic variant C/T snv 0.68 1
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs936229
ULK3
1.000 0.080 15 74839978 intron variant A/G snv 0.67 1
rs212402
LOC105378083
1.000 0.080 6 159051263 intron variant G/A snv 0.66 3
rs4675374
ICOS ; LOC101927840
0.882 0.200 2 203937855 intron variant T/C snv 0.65 5
rs7616215
CCR3 ; LOC105377067
0.925 0.280 3 46164194 intron variant C/T snv 0.62 2
rs2030519
LPP
0.827 0.200 3 188402113 intron variant G/A snv 0.61 1
rs231804 0.925 0.200 2 203843923 intergenic variant C/T snv 0.60 3
rs10903122 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 5
rs2561288
IL12A-AS1
1.000 0.080 3 159957140 intron variant T/C snv 0.54 1
rs1468788
SLC9A4
1.000 0.080 2 102476054 intron variant C/T snv 0.54 1
rs296547
MROH3P
0.882 0.200 1 200923009 intron variant T/C snv 0.53 5
rs7725052 0.716 0.240 5 40487168 intron variant C/T snv 0.52 1