Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1250563
ZMIZ1
0.724 0.240 10 79287626 intron variant G/C snv 0.24 14
rs1250552
ZMIZ1
0.882 0.200 10 79298270 intron variant A/C;G snv 1
rs2298428
YDJC
0.807 0.240 22 21628603 missense variant C/T snv 0.27 0.18 3
rs10494079
VAV3
0.882 1 107832253 intron variant G/C snv 9.0E-02 4
rs5754100
UBE2L3
0.882 22 21561877 intron variant T/C snv 0.18 5
rs4821112
UBE2L3
22 21610472 intron variant G/A snv 0.21 1
rs5754217
UBE2L3
0.925 0.120 22 21585386 intron variant G/T snv 0.31 1
rs12482947
UBASH3A
0.851 0.040 21 42431928 intron variant T/C snv 0.57 5
rs11203203
UBASH3A
0.807 0.240 21 42416077 intron variant G/A snv 0.28 4
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 20
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 7
rs35018800
TYK2
0.790 0.160 19 10354167 missense variant G/A snv 4.6E-03 4.9E-03 5
rs4648356
TTC34
1.000 0.080 1 2792599 intron variant C/A snv 0.39 1
rs2076530
TSBP1-AS1 ; BTNL2
0.724 0.640 6 32396039 missense variant T/C snv 0.42 0.40 1
rs33980500
TRAF3IP2-AS1 ; TRAF3IP2
0.742 0.200 6 111592059 missense variant C/T snv 8.6E-02 9.7E-02 3
rs3761847
TRAF1
0.827 0.200 9 120927961 intron variant G/A snv 0.52 1
rs11675342
TPO
0.851 0.040 2 1403856 intron variant C/T snv 0.40 5
rs10488631
TNPO3
0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 7
rs4958881
TNIP1
0.827 0.280 5 151070675 intron variant T/C snv 0.21 2
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 15
rs6478109
TNFSF15
0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 2
rs374039502
TNFSF13B
0.925 0.160 13 108308037 3 prime UTR variant T/A snv 2.0E-02 1
rs1800693
TNFRSF1A
0.776 0.360 12 6330843 non coding transcript exon variant T/C snv 0.36; 4.0E-06 0.38 3
rs34557412
TNFRSF13B
0.763 0.240 17 16948873 missense variant A/G snv 3.5E-03 3.9E-03 4
rs1032129
TNFRSF11B
0.851 0.040 8 118939661 intron variant A/C snv 0.37 5