Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1655558
ITPKA
0.925 0.080 15 41495387 intron variant T/G snv 0.66 3
rs59185885
IL1RL1 ; IL18R1
1.000 0.040 2 102327786 intron variant T/G snv 0.18 2
rs112119265
CARD11
7 3022995 intron variant T/G snv 5.2E-02 1
rs2197415 10 9020893 intergenic variant T/G snv 0.66 1
rs1800440
CYP1B1
0.653 0.440 2 38070996 missense variant T/C;G snv 0.15; 4.0E-06 6
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 8
rs3749833
IRF1-AS1
0.925 0.080 5 132463934 non coding transcript exon variant T/C snv 0.23 4
rs2255088
PRKCQ-AS1
1.000 0.040 10 6583416 intron variant T/C snv 0.39 2
rs75130836 11 76180138 intergenic variant T/C snv 1.2E-02 2
rs4713841 6 35189310 intergenic variant T/C snv 0.28 1
rs7134784
PLXNC1
12 94188701 intron variant T/C snv 0.83 1
rs9611602
ACO2
22 41512401 intron variant T/C snv 0.19 1
rs9828592
GLB1
3 33002847 intron variant T/C snv 0.49 1
rs1420466 3 169000309 upstream gene variant T/A;G snv 1
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 11
rs30526
SEPTIN8
5 132774274 intron variant T/A;C snv 1
rs3939286 0.776 0.360 9 6210099 regulatory region variant T/A;C snv 1
rs72925996
BACH2
6 90220794 intron variant T/A;C snv 1
rs112401631 0.882 0.120 17 40608272 TF binding site variant T/A snv 1.1E-02 8
rs9889262
ZNF652
17 49320708 intron variant T/A snv 0.28 3
rs7936312 0.882 0.080 11 76582682 intergenic variant G/T snv 0.44 5
rs8020739 14 35413286 TF binding site variant G/T snv 0.67 2
rs11178649
TSPAN8
12 71139458 intron variant G/T snv 0.32 1
rs57347370
GJA1
6 121440942 intron variant G/T snv 0.25 1
rs6473228 8 80387531 intron variant G/T snv 0.59 1