Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12712127
IL1R1
2 102110201 intron variant A/G snv 0.62 3
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs6734238 1.000 0.080 2 113083453 upstream gene variant A/G snv 0.39 4
rs270607
MIR3936HG ; SLC22A4
5 132313493 intron variant A/G snv 0.69 3
rs12777
MIR3936HG ; SLC22A4
5 132335969 synonymous variant C/G snv 3.1E-02 2.8E-02 3
rs2073643
SLC22A5
1.000 0.080 5 132387596 intron variant T/C snv 0.46 4
rs1016988 5 132408882 upstream gene variant T/C snv 0.20 3
rs11242111
LINC02863 ; IRF1-AS1
5 132420366 intron variant A/G;T snv 3
rs2106854
IRF1-AS1
5 132433482 intron variant C/T snv 0.23 3
rs6874639
IRF1-AS1
5 132443024 intron variant A/G snv 0.24 3
rs2522056
IRF1-AS1
5 132466034 intron variant G/A snv 0.25 3
rs6873426
IRF1-AS1 ; IRF1
5 132482939 3 prime UTR variant G/T snv 0.38 3
rs17690122 5 132532143 intron variant A/G;T snv 3
rs743562 5 132536691 intron variant C/T snv 0.35 3
rs2158177
TH2LCRR
0.925 0.120 5 132648366 intron variant A/G snv 0.18 4
rs3091307
TH2LCRR
0.925 0.160 5 132653444 intron variant A/G snv 0.34 3
rs1154988 3 136206349 upstream gene variant T/A snv 0.76 3
rs511154 3 136232079 intergenic variant A/G;T snv 3
rs7464572
MIR661 ; PLEC
8 143946999 intron variant C/A;G snv 3
rs12651106
DCHS2
4 154379907 intron variant C/A snv 0.12 3
rs7518199
IL6R
1 154434943 intron variant A/C;T snv 0.39; 4.2E-06 4
rs4537545
IL6R
0.790 0.160 1 154446403 intron variant C/T snv 0.48 4
rs7529229
IL6R
0.851 0.120 1 154448302 intron variant T/C snv 0.48 4
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 5
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 5