Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs301805
RERE
1.000 0.080 1 8420956 intron variant T/G snv 0.65 3
rs36045143
LOC105371081 ; CLEC16A
1.000 0.080 16 11131109 intron variant A/G snv 0.18 3
rs4833103
TLR1
0.925 0.160 4 38813881 intron variant A/C snv 0.64 3
rs56375023
SMAD3
0.925 0.120 15 67156025 intron variant G/A snv 0.17 3
rs697852
ITPKB
1 226727033 intron variant G/A snv 0.82 3
rs9303277
IKZF3
0.790 0.240 17 39820216 intron variant C/T snv 0.52 3
rs9860547
LPP
0.925 0.080 3 188411191 intron variant G/A snv 0.34 3
rs9889262
ZNF652
17 49320708 intron variant T/A snv 0.28 3
rs10074523
KIF3A
1.000 0.080 5 132724891 intron variant C/A snv 0.62 2
rs10197862
IL18R1 ; IL1RL1
0.925 0.120 2 102350089 intron variant A/G snv 0.18 2
rs10208293
IL1RL1 ; IL18R1
0.882 0.160 2 102349850 intron variant G/A snv 0.33 2
rs10445308
IKZF3
0.851 0.240 17 39781794 intron variant C/T snv 0.38 2
rs10947428
ITPR3
1.000 0.040 6 33679281 intron variant T/C snv 0.26 2
rs11169225
AQP2 ; LOC101927318
1.000 0.120 12 49951888 intron variant T/A snv 0.13 2
rs11645657
LOC105371081 ; CLEC16A
1.000 0.080 16 11129597 intron variant C/A;G snv 0.48 2
rs11684176
PLCL1
2 198090050 intron variant C/T snv 0.38 2
rs12339348
LOC107987046 ; IL33
1.000 0.080 9 6233082 intron variant A/G;T snv 2
rs12743520
EVI5
1.000 0.080 1 92571555 intron variant C/A snv 0.20 2
rs12935657
CLEC16A
0.925 0.080 16 11125184 intron variant G/A snv 0.18 2
rs13001325
IL18R1 ; IL1RL1
1.000 0.040 2 102322576 intron variant C/T snv 0.30 2
rs13099273
LPP
1.000 0.080 3 188415730 intron variant A/G;T snv 2
rs13416555
LINC00299
1.000 0.080 2 8301605 intron variant C/A;G snv 2
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 2
rs146668528
HLA-DQA1
1.000 0.080 6 32630251 intron variant C/T snv 5.7E-02 2
rs148906978
TLR1 ; TLR6
1.000 0.080 4 38852748 intron variant C/T snv 0.29 2