Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2030519
LPP
0.827 0.200 3 188402113 intron variant G/A snv 0.61 7
rs114558062 0.851 0.040 3 187923342 intergenic variant T/C snv 6.6E-03 5
rs10937560
MB21D2
0.882 3 192909627 intron variant G/C snv 0.45 4
rs145268310 0.882 3 12269274 regulatory region variant G/C snv 9.9E-02 4
rs1530687
ARHGAP31
0.882 3 119395668 intron variant G/A snv 0.46 4
rs1921445 0.882 3 106229671 intergenic variant A/C;G snv 4
rs28583049
LOC105374033
0.882 3 108724568 downstream gene variant T/C snv 0.17 4
rs57791671 0.882 3 121889586 upstream gene variant T/A snv 0.38 4
rs62324212
IL21-AS1
0.724 0.240 4 122639784 intron variant C/A;G snv 15
rs7660520 0.724 0.240 4 182824168 upstream gene variant G/A;C snv 14
rs7672495 0.724 0.240 4 4990640 regulatory region variant T/C snv 0.21 14
rs7441808
LINC02357
0.851 0.040 4 26088753 intron variant A/G snv 0.20 5
rs56817615
CLNK
0.882 4 10717222 intergenic variant A/G snv 0.42 4
rs6840978
IL21-AS1
0.776 0.160 4 122633552 intron variant C/T snv 0.16 4
rs7655915
LOC107986195
0.882 4 148712316 intron variant C/T snv 0.22 4
rs9683415 0.882 4 40290296 regulatory region variant A/G snv 0.71 4
rs7725052 0.716 0.240 5 40487168 intron variant C/T snv 0.52 15
rs7731626
ANKRD55
0.716 0.240 5 56148856 intron variant G/A snv 0.30 15
rs11741255
IRF1-AS1
0.724 0.240 5 132475490 intron variant G/A snv 0.29 14
rs4869313
ERAP2 ; ERAP1
0.724 0.240 5 96888176 intron variant T/A;G snv 14
rs755374 0.724 0.240 5 159402286 intron variant C/T snv 0.28 14
rs114378220
CAMK4
0.851 0.040 5 111230662 intron variant C/T snv 4.5E-02 5
rs11746555
SLC22A5
0.882 5 132391341 intron variant G/A snv 0.28 4
rs1549922 0.882 5 159304540 intergenic variant G/A snv 0.56 4
rs391851 0.882 5 103342219 intergenic variant A/C;G;T snv 4