Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7863183
DELEC1
0.925 0.080 9 114880138 intron variant T/A;C snv 2
rs2974
TNFSF8 ; DELEC1
1.000 0.040 9 114901892 intron variant T/C snv 0.56 1
rs2295800
TNFSF8 ; DELEC1
1.000 0.040 9 114901931 intron variant T/C snv 0.56 1
rs3181362
TNFSF8 ; DELEC1
1.000 0.040 9 114905163 intron variant T/C snv 0.21 1
rs1322054
TNFSF8 ; DELEC1
1.000 0.040 9 114907019 intron variant A/G snv 0.58 1
rs3789882
DELEC1 ; TNFSF8
1.000 0.040 9 114907419 intron variant A/T snv 0.22 1
rs3789879
DELEC1 ; TNFSF8
1.000 0.040 9 114915956 intron variant T/C snv 0.58 1
rs1885383
TNFSF8 ; DELEC1
1.000 0.040 9 114917522 intron variant G/A snv 0.21 1
rs3181360
DELEC1 ; TNFSF8
1.000 0.040 9 114929278 intron variant C/A;T snv 1
rs254079
SEMA6A
1.000 0.040 5 116555387 intron variant A/G snv 0.49 1
rs495662 1.000 0.040 6 117802987 intergenic variant G/A snv 0.92 1
rs6421571 0.851 0.200 11 118873063 intergenic variant T/A;C snv 3
rs2073617
COLEC10 ; TNFRSF11B
0.776 0.360 8 118952044 upstream gene variant G/A snv 0.58 1
rs10886462
GRK5
1.000 0.040 10 119345799 intron variant A/G snv 0.22 1
rs3897478 1.000 0.040 1 119908567 downstream gene variant T/C snv 0.17 1
rs11938795
KIAA1109
0.882 0.120 4 122151854 upstream gene variant T/C snv 0.24 1
rs7657746
KIAA1109
0.925 0.040 4 122240464 intron variant A/G snv 0.24 1
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 5
rs13132308
IL21-AS1
0.807 0.160 4 122629959 intron variant A/G snv 0.10 1
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 1
rs921720
LOC105375746
1.000 0.040 8 125522429 intron variant A/G snv 0.48 2
rs4871611
LOC105375746
1.000 0.040 8 125525328 intron variant G/A snv 0.48 1
rs1551398
LOC105375746
0.882 0.160 8 125527809 intron variant G/A snv 0.48 3
rs9491697
RSPO3
1.000 0.040 6 127134977 intron variant A/G snv 0.41 1
rs226534 1.000 0.040 X 127768516 intergenic variant A/G snv 0.34 1