Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs221781 0.882 7 100698285 upstream gene variant A/G;T snv 4
rs2075184 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 14
rs391851 0.882 5 103342219 intergenic variant A/C;G;T snv 4
rs1320344
C12orf42
0.882 12 103493699 intron variant A/G snv 0.64 4
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 20
rs62131887 0.724 0.240 19 10476920 intergenic variant C/T snv 0.37 14
rs10444776
LOC112268138
0.882 14 105647030 upstream gene variant G/A;T snv 4
rs1921445 0.882 3 106229671 intergenic variant A/C;G snv 4
rs11839053 0.724 0.240 13 106410694 intergenic variant T/C snv 7.0E-02 14
rs56817615
CLNK
0.882 4 10717222 intergenic variant A/G snv 0.42 4
rs10494079
VAV3
0.882 1 107832253 intron variant G/C snv 9.0E-02 4
rs28583049
LOC105374033
0.882 3 108724568 downstream gene variant T/C snv 0.17 4
rs114378220
CAMK4
0.851 0.040 5 111230662 intron variant C/T snv 4.5E-02 5
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12
rs191252491
ALDH2
0.882 12 111773070 intron variant A/T snv 7.1E-03 4
rs8061370
LOC105371082 ; RMI2
0.882 16 11364614 intron variant A/C;T snv 4
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 25
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 15
rs1032129
TNFRSF11B
0.851 0.040 8 118939661 intron variant A/C snv 0.37 5
rs1530687
ARHGAP31
0.882 3 119395668 intron variant G/A snv 0.46 4
rs13299616
PSMD5 ; CUTALP
0.882 9 120832525 intron variant T/C snv 0.50 4
rs57791671 0.882 3 121889586 upstream gene variant T/A snv 0.38 4
rs7088058
PLEKHA1
0.851 0.040 10 122389836 intron variant C/T snv 0.32 4
rs6840978
IL21-AS1
0.776 0.160 4 122633552 intron variant C/T snv 0.16 4