Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs343490 9 6064575 intron variant A/C;G snv 1
rs6909461 6 31386173 upstream gene variant A/C;G snv 1
rs391755
NOTCH4
1.000 0.120 6 32224659 upstream gene variant A/C;G;T snv 0.11 2
rs13019081
IL18R1 ; IL1RL1
2 102334362 intron variant A/C;G;T snv 1
rs1553575 5 40502830 intron variant A/C;G;T snv 1
rs16924428 9 6351111 intergenic variant A/C;G;T snv 1
rs17553936
WDR36
5 111118983 intron variant A/C;G;T snv 0.33 0.26 1
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 5
rs11903129
PLCL1
2 198053867 intron variant A/C;T snv 1
rs17756142
LOC107987046
9 6301578 intergenic variant A/C;T snv 1
rs3771164
IL18R1
2 102375326 intron variant A/C;T snv 1
rs3860069 4 38860500 upstream gene variant A/C;T snv 1
rs6749114
IL18R1 ; IL1RL1
2 102351127 intron variant A/C;T snv 1
rs7603730
IL18R1
2 102357911 intron variant A/C;T snv 1
rs7735058
TTC33
5 40555036 intron variant A/C;T snv 1
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 12
rs8067378 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 6
rs9391858
TSBP1-AS1 ; TSBP1
0.925 0.080 6 32373621 intron variant A/G snv 0.13 6
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 5
rs7751725 1.000 6 31392656 downstream gene variant A/G snv 0.31 5
rs176095
PBX2 ; GPSM3
0.925 0.160 6 32190542 upstream gene variant A/G snv 0.22 3
rs204993
PBX2
0.851 0.240 6 32187804 intron variant A/G snv 0.24 0.26 3
rs3091307
TH2LCRR
0.925 0.160 5 132653444 intron variant A/G snv 0.34 3
rs3816470
IKZF3
0.925 0.160 17 39829548 intron variant A/G snv 0.54 3
rs7130588 0.882 0.200 11 76559639 regulatory region variant A/G snv 0.29 3